Clinical trials

12

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Condition / disease
Location
Status: Recruiting

Predictors of Transmural Non-Occlusive Mesenteric Ischemia in ICU Patients With Suspected Acute Mesenteric Ischemia

Acute mesenteric ischemia (AMI) is a rare but life-threatening condition associated with high mortality and major diagnostic challenges due to nonspecific clinical presentation and limited reliable biomarkers. Critically ill patients in the intensive care unit (ICU) are at particularly high risk of non-occlusive mesenteric ischemia (NOMI), a subtype of AMI characterized by impaired mesenteric perfusion without large-vessel occlusion. Despite advances in imaging, the diagnosis of NOMI remains difficult, and data specifically focusing on ICU patients with suspected AMI are limited. This prospective observational multicenter study aims to identify independent predictors of transmural NOMI among ICU patients with suspected AMI. In addition, the study will describe demographics, comorbidities, clinical presentation, laboratory findings, diagnostic imaging, management strategies, and outcomes among ICU patients with NOMI, other forms of AMI, and patients with suspected but unconfirmed AMI. Consecutive adult ICU patients in whom clinical suspicion of AMI arises during ICU stay will be included across Estonian regional hospitals. The study is a local continuation of the international AMESI study, with a specific focus on critically ill ICU patients.

Participants needed: 150
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University of TartuUpdated: May 28, 2026Locations: 2
Eligibility criteria

Patients who develop acute mesenteric ischemia outside of the intensive care uni... [+3]

Status: Recruiting

The Effect of Playful Physiotherapy Intervention

The goal of this quasi-experimental study is to evaluate the changes in emotional, behavioral, and psychosocial functioning of children aged 7-12 following a playful physiotherapy intervention. The study focused on the potential effects of a play- and body-based intervention on children's daily functioning, based on parent-reported assessments The main question\[s\] it aims to answer \[is/are\]: Participants will be evaluated based on the Strengths and Difficulties Questionnaire and KIDSCREEN-27 before and after the playful physiotherapy intervention programme.

Participants needed: 25
Trial details
Age: 7-12Biological sex: AllType: InterventionalSponsor: University of TartuUpdated: May 5, 2026Locations: 1
Eligibility criteria

Age 5-12 years; [+5]

Acute or chronic medical condition that prevents active participation; [+2]

Status: Recruiting

The Effect of Pain Education Group Therapy and Its Impact on Chronic Pain, Kinesiophobia, and Physical Activity

The goal of this clinical trial is to learn if pain knowledge group intervention among chronic pain patients would influence their level of physical activity, pain intensity, depression, kinesiophobia and central sensitization. The main question it aims to answer is: Primary hypothesis: pain education will decrease participants' depression and pain intensity and increase their physical activity. There is no comparison group. Participants will participate in a 6-week pain knowledge intervention where they will be learning about sleep, stress models, physical activity benefits, pain neurobiology, mindfulness, pain medication.

Participants needed: 50
Trial details
Age: 16-65Biological sex: AllType: InterventionalSponsor: University of TartuUpdated: Mar 30, 2026Locations: 1
Eligibility criteria

Pain lasting longer than 3 months, [+1]

Surgery that occurred less than 3 months prior [+1]

Status: Recruiting

Central Haemodynamics and Pacing for AV Block

A randomized, single-blind study comparing two pacing strategies in patients with atrioventricular block requiring permanent pacemaker implantation. This trial evaluates the impact of conduction system pacing (left bundle branch area pacing) versus standard right ventricular pacing on central hemodynamics, cardiac function, and patient quality of life over 12 months. The study will enroll 124 patients from two Estonian tertiary hospitals and measure central systolic arterial pressure as the primary outcome, with secondary assessments of arterial stiffness, echocardiographic parameters, electrical activation patterns, and quality of life scores.

Participants needed: 124
Trial details
Age: 18-80Biological sex: AllType: InterventionalSponsor: University of TartuUpdated: Mar 9, 2026Locations: 2
Eligibility criteria

Age 18-80 years [+2]

Reduced left ventricular ejection fraction (EF <45%) [+11]

Status: Recruiting

Study About Contrast Media

Patients hospitalized with adhesive small bowel obstruction (SBO) are randomized to 2 study groups at admission after signing an informed consent form. Water-soluble contrast media (CM) will be administered after 4 or after 24 hours of nasogastric- tube decompression.

Participants needed: 120
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of TartuUpdated: Mar 30, 2025Locations: 1
Eligibility criteria

Patients 18 years or older [+3]

Patients younger than 18 yeas [+5]

Status: Recruiting

The Feasibility of a Radiological Score Based on CT Signs for Recognizing Salvageable Bowel in Acute Mesenteric Ischemia

Computed tomography (CT) is the standard modality for scanning patients with critical acute abdominal conditions, including suspected acute mesenteric ischemia (AMI). CT imaging can potentially differentiate between reversible and irreversible ischaemic damage of the bowel. This moment is pivotal in selecting the treatment strategy for AMI - in the absence of irreversible damage; reperfusion therapy can preserve intestinal viability, thereby avoiding the need for bowel resection. The present study tests the hypothesis that combining several symptoms may enhance the diagnostic performance of CT scanning in detecting salvageable bowel in patients with AMI. This study is an ancillary component of the AMESI study (Clinical Trials: NCT05218863) - a prospective, multicentre observational study aimed at identifying the incidence and describing the outcomes of acute mesenteric ischemia (AMI) in adult hospitalized patients. The ultimate purpose of the present study is to create a computed tomography-based radiological score for the assessment of bowel viability in patients with AMI.

Participants needed: 200
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University of TartuUpdated: Mar 25, 2025Locations: 1Duration: 1 Year
Eligibility criteria

Participant in AMESI study [+2]

Scans without the use of an intravenous contrast media or those covering only a...

Status: Recruiting

Effect of Psychedelic VR-augmented Therapy on Patients With Clinical Depression

Research has demonstrated that psychedelic compounds possess significant therapeutic potential for a variety of disorders, including depression. Despite these findings, the underlying mechanisms driving the therapeutic efficacy of psychedelics remain elusive. Furthermore, there exists a debate over the contribution of the subjective psychedelic experience to their therapeutic benefits. In this study, virtual reality (VR) is utilized as a tool to replicate the subjective experiences induced by psychedelics, aiming to explore their impact on depressive symptoms within a clinical sample. The primary objective of this research is to examine the influence of psychedelic-like phenomenology, as simulated through VR, on depressive symptoms. The study is structured into two distinct arms: the experimental condition features 'Psyrreal,' a VR experience designed to emulate psychedelic effects and the control condition which includes 'Routine Realms,' an analogous VR experience devoid of psychedelic elements. A third waiting list condition may be included, dependent on the availability of sufficient participants and resources. Additionally, the study seeks to identify and analyze various potential mediators that might underpin the therapeutic outcomes observed.

Participants needed: 45
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: University of TartuUpdated: Mar 25, 2025Locations: 1
Eligibility criteria

Persistent depressive symptoms observed during the initial screening and confirm... [+2]

Presence of significant impairments in vision, hearing, or balance. [+6]

Status: Recruiting

Standardising and Simplifying the Global Leadership Initiative on Malnutrition (GLIM) for Its More General Application

This observational study of aims to test whether and how the results of GLIM change when using different approaches and methods to carry out its components.

Participants needed: 300
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University of TartuUpdated: Mar 28, 2025Locations: 1
Eligibility criteria

Age of 18+ years [+3]

Age of <18 years [+4]

Status: Recruiting

Integrating BIA and eGFR for Nutritional Status in Hemodialysis Patients

This study looks at how measurements of body composition from Bioelectrical Impedance Analysis (BIA) and estimates of kidney function (eGFR) can be applied together to better assess the health of people on hemodialysis. Many dialysis patients struggle with malnutrition, muscle loss, and fluid imbalances, but current assessment methods rely on unsophisticated tests and observations. By combining BIA and eGFR, this study aims to provide a more accurate and non-invasive way to monitor nutrition and overall health, which could lead to better treatment decisions and improved patient outcomes.

Participants needed: 30
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University of TartuUpdated: Mar 13, 2025Locations: 1
Eligibility criteria

Not listed

Status: Not yet recruiting

Calf Circumference Adjusted for Body Composition to Assess Muscle Mass

Muscle mass is a critical indicator for malnutrition and sarcopenia assessment. Anthropometric measurements like calf circumference (CC) could be a simple and cost-effective alternative when gold standard methods are not available. However, CC is probably less accurate for estimating muscle mass in female patients and patients with obesity. This study investigates whether adjusting CC using mid-upper arm circumference (MUAC) improves muscle mass estimation in patients with obesity. If validated, this correction method would serve as a simple clinical tool for muscle mass assessment.

Participants needed: 150
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University of TartuUpdated: Feb 17, 2025
Eligibility criteria

Not listed

Status: Recruiting

Biomarkers in Prediction of AMI

Current study will be undertaken to identify combinations of biomarkers that can reliably identify acute mesenteric ischaemia (AMI) and distinguish between non-transmural and transmural ischaemia. Different combinations of biomarkers for different sub-types and severity of AMI, and different time points of measurement after onset of symptoms.

Participants needed: 250
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of TartuUpdated: Dec 3, 2024Locations: 2
Eligibility criteria

Age 18 years or older [+1]

Age <18 years [+5]

Status: Recruiting

Effects of Remote Ischaemic Preconditioning in Cemented Hip Arthroplasty.

Total joint arthroplasty is one of the best treatment options for end-stage osteoarthritis. Cemented hip arthroplasty is mainly indicated for elderly patients with poor bone quality and multiple comorbidities. Bone cement implantation syndrome is associated with cemented hip arthroplasty and it has been shown to increase cardiovascular and renal complication and brain damage postoperatively. The aim of this project is to elucidate whether remote-ischemic preconditioning (RIPC) has multi-organ protective effect in cemented hip arthroplasty patients.

Participants needed: 200
Trial details
Age: 65-90Biological sex: AllType: InterventionalSponsor: University of TartuUpdated: Apr 4, 2024Locations: 1
Eligibility criteria

age >65 years [+1]

previously diagnosed peripheral artery disease on both upper limb [+1]