Clinical trials

176

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Condition / disease
Location
Status: Recruiting

Pilot Study: Home Use of Wearable Grasping Neuroprosthesis in Vascular Hemiparesis

Stroke is the leading cause of acquired motor disability in adults. Six months post-stroke, 50% of patients have not regained active finger extension, and 80% retain a grasping deficit, most commonly an inability to actively open the hand. This motor impairment significantly impacts daily activities, social interactions, professional life, and overall quality of life. Despite numerous treatments available in rehabilitation centers during the subacute phase, no functional assistive devices are currently usable at home. Since 2018, our team, in collaboration with the CAMIN-INRIA team, has developed a Grasp Neuroprosthesis (GNP). This device uses functional electrical stimulation to restore grasping function in hemiplegic subjects, enhancing autonomy in daily bimanual tasks. The GNP has been evaluated in hospital settings through two studies, defining preferred control modalities and demonstrating significant functional impact. Additionally, another study tested a wearable version of the GNP used autonomously at home for two months. This study showed the feasibility and functional benefits of home GNP use, provided the device is customizable to the patient's characteristics and environment. Initial results indicate improved quality of life and increased autonomy with GNP use. The wearable GNP consist of a forearm orthosis made of soft fabric, integrating an electrode array and a stimulator (CE medical marking for home use), connected via WiFi to a microprocessor positioned in a pouch. The microprocessor incorporates information from inertial measurement units and a microphone, allowing the user to control the electrical stimulator on demand. The stimulation targets the extensor muscles of the long fingers and the thumb, enabling the user to open the hand on demand. We propose extending the home use of the GNP to two patients for one year. Each subject will be followed for one year, with evaluations in a hospital setting at the beginning and end of the period, monthly follow-ups at home throughout the year, and on-demand video consultations.

Participants needed: 2
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Jun 30, 2026Locations: 2
Eligibility criteria

Adult patient who participated in and completed the GRASP-AGAIN study and achiev... [+8]

The person is in labor or breastfeeding; [+17]

Status: Not yet recruiting

Biological Collection on Emerging Infectious Diseases and Their Treatments

Unprecedented changes in human-environment interactions and increasing disruptions to ecosystems and the climate have contributed to the emergence of infectious diseases (Emerging Infectious Diseases, EIDs). Advances in the treatment of cancers, malignant haematological disorders and immune-mediated inflammatory diseases are also contributing to the creation of new infectious risks among immunocompromised patient populations. The COVID-19 pandemic has shown that structuring research prior to any outbreak is essential for the rapid implementation of responses to the emergence of an EID. The unpredictability of an EID's occurrence necessitates the planning of research projects in advance. A key element in this planning is the development of a collection of biological samples, providing a structured and immediately deployable resource for conducting pathophysiological and therapeutic research aimed at: * Analyze the biological determinants of the microbe and the resulting infection * Develop new tools for identification and characterization * Study the factors (biomarkers/signatures) associated with individual patient susceptibility and response to treatment (personalized medicine) * Understand the pathophysiology of infection to identify new targets for diagnostic, curative and preventive treatment * Monitor the efficacy of curative and preventive treatments

Participants needed: 5,300
Trial details
Age: 18-99Biological sex: AllType: ObservationalSponsor: University Hospital, ToulouseUpdated: Jun 29, 2026Locations: 1Duration: 10 Years
Eligibility criteria

Patients aged 18 years or over [+4]

Status: Not yet recruiting

Platelets and Extracorporeal Membrane Oxygenation Veno-venous

In severe lung or heart disease, ExtraCorporeal Membrane Oxygenation (ECMO) may be used temporarily and can be responsible for major haemorrhagic complications. Thrombocytopenia and possibly thrombopathy promote bleeding. The primary objective is to characterize platelet dysfunction by aggregometry tests over time. Secondarily, investigators seek a correlation between haemorrhagic complications at day 10 and markers of platelet action and dysfunction; also, with the level of anticoagulation and inflammation by biomarkers.

Participants needed: 40
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University Hospital, ToulouseUpdated: Jun 29, 2026Locations: 1
Eligibility criteria

Adults aged ≥ 18 years [+7]

Minors [+9]

Status: Recruiting

Combined Whole-brain Structural and Functional MRI for the Prediction of Neurological Recovery After Cardiac Arrest

To assess the performance of a predictive model resulting from the analysis of sMRI/fMRI/contrast-enhanced MRI-derived personalized connectomic data, as compared with standard predictors (clinical examination, electrophysiology, serum biomarker, standard neuroimaging) collected ≥ 72h from sedation withdrawal and in normothermia condition, to predict anoxoischemic coma neurological outcome at 6 months.

Participants needed: 263
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Jun 29, 2026Locations: 1
Eligibility criteria

Adult patients (male or female ≥ 18 years). [+4]

Brain death. [+11]

Status: Not yet recruiting

Measuring the Evolution of Speech Perception in Noise, in Realistic Sound Environments According to Age

In clinical settings, hearing perception is typically assessed using audiometric tests administered in a controlled environment. To date, these tests are administered in silence or in the presence of noise from fixed sources at an arbitrarily predetermined signal-to-noise ratio. These assessment situations are not representative of the functional difficulties encountered by people with hearing loss or Auditory Processing Disorder in their daily lives. In real life, "soundscapes" are diverse. Hearing assessment and rehabilitation should include the child's everyday environments as well as their lifestyle habits. The Immersion 360 System (Virtual reality system) was developed specifically to virtually reproduce complex everyday sound experiences with realistic noise types and sound presentation conditions, enabling the assessment of auditory perception under test conditions similar to those encountered in daily life. Some of the sound environments offered by this innovative system have been standardized for adults. No standards exist for children, and we have limited knowledge regarding the development of speech perception skills in noise during childhood and adolescence. It seems essential to measure the age-related development of speech perception in realistic sound environments in order to establish reference data for children and adolescents. This work will, through functional assessments of the auditory system and linguistic tests (speech perception in noise), provide a better understanding of the functional development of the central auditory system for speech perception in noise. The results collected from normo-hearing individuals in the age groups of interest will provide a clinical baseline for comparison with patients of the same age.

Participants needed: 150
Trial details
Age: 7-15Biological sex: AllType: ObservationalSponsor: University Hospital, ToulouseUpdated: Jun 30, 2026Locations: 1
Eligibility criteria

Children with normal hearing (average hearing thresholds at 250 Hz, 500 Hz, 1000... [+6]

Inability of the child to respond to tests [+9]

Status: Recruiting

Allogeneic Adipose Tissue Derived-stem Cells in Alzheimer Disease

A3D is a phase I/II clinical trial. The primary objective is to evaluate the safety of allogeneic adipose tissue derived-stem cells (AdMSC) administered by intravenous (IV) route in mild to moderate Alzheimer disease (AD) using a dose escalation protocol.

Participants needed: 9
Trial details
Phase: Phase 1, Phase 2Age: 50-85Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Jun 23, 2026Locations: 1
Eligibility criteria

Patient between 50 and 85 years old [+5]

Brain disease (other than AD) that may cause dementia [+10]

Status: Recruiting

Radiofrequency Ablation Versus Adrenalectomy for Adenoma in Patients With Primary Aldosteronism and Hypertension

Primary aldosteronism (PA) is characterized by hypertension, frequent hypokalaemia, and an inappropriately high aldosterone-to-renin ratio (ARR). Aldosterone-producing adenoma (APA or Conn syndrome) is one of the main causes of primary aldosteronism. Laparoscopic (LA) total-adrenalectomy or adenoma selective is an option to normalize or at least improve blood pressure (BP) control, hypokalaemia, and normalize the ARR. However, the reported result of surgery is around 50% of clinical cure rate with an overall complication rate of 5 to 14% whereas hormonal success reached around 95%. More recently, radiofrequency ablation (RFA) has been used for patients with primary aldosteronism and unilateral adenoma. Investigator Team assume that treatment of unilateral PA by RFA could achieve similar efficacy to treatment by LA, with potentially less adverse events, and could be a more cost-efficient procedure.

Participants needed: 134
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Jun 11, 2026Locations: 1
Eligibility criteria

Patient over 18 years of age [+9]

a negative lateralization of secretion on adrenal venous sampling [+19]

Status: Recruiting

Clinico-biological Collection of Bone, Calcium and Growth Plate Pathologies

The aim of this project is to set up a biological and clinical collection of patients with progressive bone, calcium and growth plate pathologies. This collection will provide a better understanding of the mechanisms involved in growth plate and bone damage in these diseases and identify factors predictive of progression and new therapeutic targets.

Participants needed: 350
Trial details
Age: Up to 99Biological sex: AllType: ObservationalSponsor: University Hospital, ToulouseUpdated: Jun 5, 2026Locations: 1
Eligibility criteria

Children (from birth) with growth plate or bone pathology [+4]

Patients under legal protection (guardianship, curatorship or safeguard of justi... [+1]

Status: Not yet recruiting

The Potential of Transcutaneous Electrical Nerve Stimulation to Improve Pain Experienced During Posterior Branch Blocks in Patients With Lumbar Posterior Joint Syndrome

Procedural pain is inadequately managed in two-thirds of patients undergoing invasive medical procedures. Several techniques exist for managing procedural pain, but they all present implementation challenges and are not without side effects. Therefore, a new, non-pharmacological, inexpensive, and easy-to-use approach would be of significant benefit. Transcutaneous electrical nerve stimulation (TENS) for pain relief could represent this alternative. Few studies have been conducted on the benefits of TENS in managing procedural pain, for example, in shoulder arthrodistension. This project proposes to study it in the context of posterior ramus infiltration in patients eligible for this indication, in the context of chronic low back pain associated with posterior joint syndrome.

Participants needed: 52
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Jun 4, 2026Locations: 1
Eligibility criteria

Chronic low back pain (lasting more than 3 months) [+3]

Spinal surgery [+11]

Status: Recruiting

Non-interventional Study Exploring the Composition of the Valvular Microbiota of Patients Undergoing Cardiac Surgery

The prevalence of aortic valve disease is increasing, with these valvulopathies present in half of individuals over the age of 65. Oberbach A. et al (1) demonstrated the presence of microbiota in 52% of cases of explanted aortic valves. One current hypothesis is the role of this microbiota in the pathophysiology of these degenerative valve diseases. This microbiota is probably not completely eradicated after resection of the native valve and implantation of a conventional prosthesis; it is even left in place during percutaneous aortic valve implantation, during which the prosthesis is deployed within the native valve. It could therefore also play a role in the occurrence of postoperative complications and the degeneration or thrombosis of a bioprosthesis. Furthermore, recent clinical and epidemiological studies have shown a link between oral infections and cardiovascular diseases. As recommended by the HAS, these patients require multidisciplinary care, involving cardiologists, cardiac surgeons and general practitioners, as well as careful oral and dental care and monitoring provided by specialists in oral pathologies and oral care. The accumulation of bacterial plaque on the surface of the tooth and certain oral bacteria causes the development of periodontal pockets which are characteristic of periodontitis. Bacteria, microbial products and inflammatory mediators produced locally can then enter the bloodstream and affect distant organs such as the cardiovascular system. The recommendations of the European Society of Cardiology are therefore to carry out regular oral and dental consultations to prevent the risk of infection. Therefore, within the Toulouse University Hospital, a care network has been set up for patients with cardiovascular pathologies, in order to improve their access to dental care, screening and management of oral diseases. For the past year, patients hospitalized in the cardiology departments have been seen in consultation in the dental department of the Toulouse University Hospital.

Participants needed: 200
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Jun 1, 2026Locations: 1
Eligibility criteria

Male or female patient. [+3]

Patients infected with HIV [+3]

Status: Not yet recruiting

Chrono-restricted Diet and Physical Activity as a New Preventive Strategy for Sarcopenia in Postmenopausal Women With Obesity and Type 2 Diabetes

The aim of TIMEDIAB is to demonstrate that early TRE (eTRE) combined to late (afternoon) exercise will outperform eTRE combined to morning exercise on muscle function as primary endpoint, and glucose homeostasis as secondary endpoint

Participants needed: 45
Trial details
Age: 45-70Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Jun 1, 2026Locations: 1
Eligibility criteria

Post-menopausal women (amenorrhea for at least 12 months, confirmed by gonadotro... [+7]

Subjects on T2DM injectable medication or drugs able to induce hypoglycemia (gli... [+9]

Status: Recruiting

Study Enabling the Collection of Clinical Data Necessary for the Second Phase of Development of the Glycemic Measurement Device by Analysis of Exhaled Air

A pilot study carried out by the company ALPHA-MOS in 2017-19 showed that the analysis of volatile organic compounds contained in exhaled air could reliably predict blood glucose levels. Subsequently, the company BOYDSense, a subsidiary of ALPHA-MOS, produced the Module In a Box prototypes of portable, non-invasive volatile organic compounds analyzers that could be equipped with an on-board algorithm estimating blood glucose levels. The Toulouse University Hospital conducted the BOYDSENSE-GM study in 2021-2023, in partnership with BOYDSense, aiming to develop the first algorithm for calculating blood glucose levels based on the analysis of the breath of 100 patients living with type 2 diabetes and to carry out a first performance test of the Module In a Box prototype in 30 additional subjects with type 2 diabetes. These recent results confirmed the potential of this innovative blood glucose measurement technology and gave the first indications about the next developments needed to improve its performances. The characteristics of the air exhaled by a human are impossible to simulate. Therefore, further development of the glucose calculation algorithm requires the production of additional clinical data, supporting the carrying out of the present study.

Participants needed: 235
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Jun 1, 2026Locations: 2
Eligibility criteria

Patient living with type 2 diabete or non-diabetic individuals characterized by... [+3]

Ongoing respiratory infection. [+2]

Status: Recruiting

International Multicenter Project Comparing Radiofrequency Ablation Versus Implantable Defibrillator After Well-tolerated Ventricular Tachycardia in Ischemic Heart Disease With Minimally Impaired Ejection Fraction

Evidence for the usefulness of the defibrillator in cases of preserved left ventricular ejection fraction and well-tolerated ventricular tachycardia (without cardiocirculatory arrest or syncope) is lacking, as no previous trials have included such patients. Additionally, sudden death in this particular population is low compared to other subgroups of patients with malignant ventricular arrhythmias. On the other hand, numerous recent retrospective data show that ablation of ventricular tachycardia can reduce mortality, and also clearly reduces the number of recurrences in prospective studies. Finally, a very low rate of sudden death was observed in a multicenter European retrospective study that we conducted, including patients with well-tolerated ventricular tachycardia in structural heart disease with minimally impaired ejection fraction and benefiting from ablation without implantation of defibrillator.

Participants needed: 268
Trial details
Age: 18-90Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Jun 1, 2026Locations: 1
Eligibility criteria

ischemic heart disease with history of infarction - LVEF> 35% (measured by MRI) [+3]

transient regressive cause of ventricular tachycardia [+7]

Status: Recruiting

Home Grip Assistance Glove on the Use of the Upper Limb and Compliance Factors in Brain-injured Adults

On a functional level, performing the actions of daily life requires coordinated activity of the muscles of the upper limbs. The quality of motor recovery and/or technical assistance aimed at compensating for the movement deficit of the paretic upper limb (MSP) determines the possibilities of using the upper limb (MS) in activities of daily life. Interventions in the chronic phase of stroke aim to return home. The integration of the paretic upper limb into daily life activities is a major issue regarding the prognosis of recovery of use of the upper limb. Independence in daily life becomes an ultimate goal to take charge of. This study focuses on a new technical aid device, standard orthosis type, expanding the range of gripping gloves: the SaeboGlove in everyday environments. These MS orthoses help improve the use and function of the MSP in post-stroke adults as well as their independence and participation in society.

Participants needed: 100
Trial details
Age: 18-90Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Jun 1, 2026Locations: 1
Eligibility criteria

Patient suffering from a motor deficit of the upper limb resulting from an ische... [+7]

Patient presenting retraction or stiffness of the fingers and wrist preventing c... [+13]

Status: Recruiting

Neurofeedback-EEG Rehabilitation Protocol on Motor Recovery in the Subacute Phase Post-stroke (CUSTOM-NF-STROKE)

Neurofeedback (NF) is a procedure for providing direct sensory feedback (in the form of visual, auditory or tactile stimulation) to a patient about their brain activity when performing a cognitive or motor task. This NF aims to allow the patient to become aware of this brain activity and thus learn to modulate it voluntarily in order to improve the performance obtained on the task. The aim of the study is to compare a "standard NF" procedure to a "personalized NF" procedure designed to optimize the level of patient acceptability based on the results obtained through these questionnaires.

Participants needed: 44
Trial details
Age: 18-99Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: May 29, 2026Locations: 1
Eligibility criteria

Man, woman, over 18 years old [+6]

Minors (age < 18 years) [+10]

Status: Not yet recruiting

Evaluation of Botulinum TOXin Type A in the Treatment of Buerger's Disease

The main objective is to assess the feasibility of treatment by injecting botulinum toxin A into the hand or foot of patients with signs of critical ischemia secondary to Buerger's disease. The injection of botulinum toxin A is carried out at the end of a single session during an hospitalization. Furthermore, tolerance and effects on the disease are evaluated at 1, 3 and 6 months post injections.

Participants needed: 8
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Jun 1, 2026
Eligibility criteria

Age ≥ 18 years [+6]

History of myasthenia gravis or Eaton-Lambert syndrome [+13]

Status: Recruiting

Localization of Anatomical Structures Involved in Nodal Tachycardias by High Density Mapping.

The aim of the present work is to analyze the capacity of high resolution mapping systems to determine the precise location of the AV node and peri-nodal slow-conducting pathways, using standard recording parameters, but also off-line additional filter changes and additional techniques (conduction velocities, isochrones and dV/dt). The investigative team plan a prospective monocentric study. Detailed high resolution mapping of the Koch triangle and neighboring areas will be collected through the RHYTHMIA HDx 3D electro-anatomical mapping system and the multipolar ORION catheter. This sample will consist of 2 groups of patients: the first will include patients referred for AVNRT ablation and the second will include control patients (without AVNRT), referred for another indication requiring similar mapping system. If visualized, position of the slow pathway and AV node will be compared with the ablation areas, which will be set conventionally under fluoroscopy.

Participants needed: 20
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Jun 1, 2026Locations: 1
Eligibility criteria

Presence of underlying structural heart disease or history of atrial ablation or... [+2]

Status: Recruiting

Local Inflammation in Arrhythmogenic Right Ventricular Cardiomyopathy

The understanding of ARVC pathophysiology remains incomplete. Several clues indicate that disease progression is mediated through inflammation. The present study aim to document the feasibility of detecting the potential presence of intracardiac local inflammatory components in patients with ARVC.

Participants needed: 80
Trial details
Age: 18-99Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Jun 1, 2026Locations: 1
Eligibility criteria

Arrhythmogenic right ventricular dysplasia diagnosed (according to 2010 Task For... [+2]

Diagnostic of systemic chronic inflammatory disease [+2]

Status: Recruiting

Sexual Dysfunction in Hypertensive Women

Several studies describe the existence of an association between sexual dysfunction and high blood pressure (hypertension), most often characterized by a decrease in the number of orgasms and the existence of dyspareunia. Hypertension is a contributing factor, and nonadherence to medication could amplify it. There are several ways to assess adherence to treatment: the use of declarative questionnaires, a method not without criticism because it is subject to the subjectivity of the declaration by the patient; and drug dosages, a standard technique, although insufficiently disseminated due to the high cost and greater weight of the survey protocols. Drug non-compliance is multifactorial. In addition, it has been shown that having undesirable drug effects and / or being afraid of developing them is one of the major causes of non-compliance with antihypertensive treatments. The investigators hypothesize that DS is significantly more common among hypertensive women treated with non-observers compared to hypertensive women treated with observers. The main objective is to compare the prevalence of sexual dysfunction between a group of hypertensive women treated as observers and a group of hypertensive women treated as non-observers.

Participants needed: 348
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: University Hospital, ToulouseUpdated: Jun 1, 2026Locations: 1
Eligibility criteria

Women over 18, [+3]

Patients with bariatric surgery, [+2]

Status: Recruiting

Use of Compression Bandages in the Prevention of Post-mastectomy Lymphoceles

Lymphocele secondary to a mastectomy whether or not associated with a lymph node procedure (sentinel lymph node or axillary dissection) is an almost systematic consequence observed in the postoperative situation in this type of surgery. This can be the source of pain, skin complications, and infection with a significant impact on the length of hospitalization for patients treated for breast cancer. There is no consensus regarding the management of lymphocele. The placement of a compression bandage after mastectomy and / or axillary dissection would allow a more efficient and rapid reduction of the lymphocele and a reduction in recurrences. This would make it possible to reduce the duration of the wearing of the drain, which determines the length of hospitalization and reduce the recurrence of lymphoceles, the punctures of which can be one of the risk factors for secondary lymphedema.

Participants needed: 84
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: University Hospital, ToulouseUpdated: Jun 1, 2026Locations: 1
Eligibility criteria

Patients over 18 years old, [+2]

Recurrence of breast cancer, [+17]

Status: Recruiting

Treatment of Central Airway Stenoses Using Computer-Assisted Customized 3d Stents TATUM

Airway stenting is usually efficient to treat central airway obstruction but can lead to severe and potentially lethal complications (stent migration, obstructive granuloma, perforation, and hemoptysis). 3D customized airway stents (computer-aided conception using CT-scan data), perfectly suited to airway anatomy, should improve the tolerance and safety of airway stenting. We demonstrated in a previous pilot study, dedicated to patients with anatomically complex stenoses the safety of 3D patient-specific stents. These appealing results in highly complex situations suggest the need to evaluate these devices in more common situations. In this study we aim to test our new generation stents in all patients planned for airway stenting. After computer-assisted segmentation of airways (VGStudioMAX 3.0 software), the stenosis is virtually corrected, leading to the conception of a virtual stent (AnatomikModeling, Toulouse), allowing for the fabrication of a mold using a 3D printer. The stent is then built and sterilized (NOVATECH, Berlin) and inserted during rigid bronchoscopy. Close follow up is then conducted, including clinical evaluation after one week, three, six and 12 months; spirometry at one week, 3 months, 6 months and 12 months and chest CT-scan at one week.

Participants needed: 30
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Jun 1, 2026Locations: 1
Eligibility criteria

Age >18 years [+2]

Acute respiratory distress, mechanical ventilation [+2]

Status: Recruiting

Assessment of the Functional Impact of a Close-loop Controlled Prehension Neuroprosthesis in Post-stroke Patients

The aim of the PREHENS-STROKE study is to propose a functional replacement device to restore grip capacities in patients with hemiparesis after stroke, unable to actively open the hand to seize objects. The main objective is to evaluate the impact of the use of a self-controlled prehension neuroprosthesis on the ability to perform a standardized grasping task, consisting of grasping, relocating and releasing a glass (palmar grasp) or a spoon (key-pinch), compared to a condition without the use of the prehension neuroprosthesis.

Participants needed: 30
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Jun 1, 2026Locations: 1
Eligibility criteria

Concerning the study population: Paresis of an upper limb from a single ischemic... [+1]

Concerning the study population: The person is parturient, or is breastfeeding;... [+3]

Status: Recruiting

Prevalence and Significance of ATTR Aortic Valve Amyloidosis in Degenerative Aortic Stenosis

Cardiac amyloidosis is a restrictive cardiomyopathy with a potentially severe prognosis that can be life-threatening. It is linked in the vast majority of cases to a light chain deposition of immunoglobulin or transthyretin. Although myocardial involvement is predominant, other locations are possible: the atrioventricular conduction system, coronary arteries and valve leaflets. In systematic histological analyzes, deposits of amyloidosis infiltrating the aortic valve have been reported with a frequency of up to 74% for degenerative RA. The nature of these deposits has never been established because the immunostaining carried out all remained negative, probably due to decalcification prior to cutting. Currently, these deposits are considered to be local degenerative phenomena without clinical repercussions. However, the use of bone scintigraphy has shown a high prevalence, between 14 and 16%, of ATTR cardiac amyloidosis in patients with severe RA. The diagnosis of ATTR amyloidosis has been proven histologically in a few patients. Sequencing of the TTR gene has shown that they are mainly wild forms. In fact, the prevalence of transthyretin mutations in our local cohort is 20%. The objective of this study is to determine by proteomic analysis based on mass spectrometry, the prevalence of ATTR aortic valve amyloidosis in patients undergoing surgical valve replacement for degenerative aortic stenosis.

Participants needed: 100
Trial details
Age: 18-99Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Jun 1, 2026Locations: 1
Eligibility criteria

Patient over 18 years old [+3]

Non-degenerative aortic stenosis: bicuspid, rheumatic disease, aortic regurgitat... [+2]

Status: Not yet recruiting

Impact of Topical Aromatherapy on Postoperative Quality of Recovery After Lung Resection

The key to early surgery recovery lies in optimal and immediate control of postoperative pain. Despite standard pain management protocols, lung resection is often associated with acute, neuropathic, or chronic pain, compounded by the side effects of morphine-based treatments. In this context, aromatherapy can provide complementary support, both to alleviate pain and to improve the quality of recovery after surgery.

Participants needed: 124
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University Hospital, ToulouseUpdated: Jun 3, 2026
Eligibility criteria

Adults aged 18 years or older, [+3]

Patients with chronic pain prior to surgery [+10]