Central Sensitisation

13

Review clinical trials related to Central Sensitisation. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Sedentary Status and Multidimensional Outcomes in Fibromyalgia

Fibromyalgia syndrome (FMS) is a chronic condition characterized by widespread musculoskeletal pain, fatigue, sleep disturbances, and functional limitations. Pain, fatigue, and fear of movement often lead individuals with FMS to adopt sedentary behaviors, which may further exacerbate symptoms and reduce physical capacity. Factors such as impaired body awareness, reduced respiratory muscle strength, kinesiophobia, central sensitization, poor functional status, and sleep disturbances play an important role in disease severity and quality of life in individuals with FMS. Although physical inactivity is common in fibromyalgia, limited evidence exists regarding the differences in these multidimensional clinical parameters between sedentary and non-sedentary individuals with FMS. Therefore, the aim of this study is to compare body awareness, respiratory muscle strength, kinesiophobia, central sensitization, functional status, and sleep quality between sedentary and non-sedentary individuals diagnosed with fibromyalgia syndrome. The findings of this study may contribute to a better understanding of the impact of sedentary behavior on clinical outcomes in fibromyalgia and help guide more comprehensive and individualized rehabilitation approaches.

Participants needed: 66
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Izmir Democracy UniversityUpdated: Feb 6, 2026Locations: 1
Eligibility criteria

Sedentary Fibromyalgia Participants [+4]

Sedentary Fibromyalgia Participants [+12]

Status: Not yet recruiting

Comparison of Pain, Sensitisation, Function and Quality of Life According to Stenosis Degree in Chronic Neck Pain

The cervical spine is a structure that bears the weight of the head and has important functions, but is susceptible to mechanical stress and degenerative processes. Cervical stenosis can lead to compression of the nerve roots as a result of narrowing of the spinal canal and symptoms such as pain, numbness and weakness. Central sensitisation (CS) causes even innocuous stimuli to cause pain due to hypersensitivity of the central nervous system and negatively affects the quality of life by increasing pain intensity in individuals with chronic neck pain. Progression of cervical stenosis can lead to symptoms such as walking difficulties, loss of balance and loss of proprioception. Furthermore, CS causes patients to avoid physical activity, increasing muscle weakness and pain, which further reduces quality of life. For this reason, our study will be carried out to determine the effect of cervical stenosis on patients with neck pain whom applied to Izmir Democracy University Physical Medicine and Rehabilitation outpatient clinic and had cervical MRI. Participants' pain status, central sensitisation, sensory loss, range of motion and proprioception will be recorded. Pressure pain threshold will be measured with algometer, sensory loss will be examined with Semmes-Weinstein Monofilament (SWM) Test, joint movements and proprioception will be evaluated with Pa CROM Basic device. In addition, the effects of cervical stenosis on functional status and quality of life will be measured by questionnaires. The data obtained will be compared and analysed with appropriate statistical methods. This study is aimed to contribute to the development of treatment methods and improvement of patient care, and will provide important information in terms of pain management and improvement of quality of life.

Participants needed: 88
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Izmir Democracy UniversityUpdated: Jan 5, 2026Locations: 1
Eligibility criteria

Cases whose stenosis classification can be clearly determined on MRI [+1]

Individuals who did not agree to participate in the study [+6]

Status: Recruiting

Effect of Boswellia Serrata on Pain Intensity, Central and Peripheral Sensitization, and Pain Modulation in Healthy Volunteers

This planned study is based on a randomized, placebo-controlled cross-over design. Boswellic acids, the triterpenes found in the gum resins of Boswellia serrata (family: Burseraceae), are traditionally used in the Indian Ayurvedic medicine system as antioxidants and anti-inflammatory agents for treating conditions such as rheumatoid arthritis, chronic bronchitis, asthma, and chronic inflammatory bowel diseases (ulcerative colitis and Crohn's disease). The β-configured pentacyclic triterpenic acids in B. serrata include 3-acetyl-11-keto-β-boswellic acid (AKBBA), 11-keto-β-boswellic acid (KBBA), β-boswellic acid (BBA), and 3-acetyl-β-boswellic acid (ABBA). These compounds, which constitute approximately 14% of the lipophilic fractions of the B. serrata extract, are the major active components. Boswellia serrata is marketed as a food supplement in accordance with EU Directive 2002/46/EC. Several clinical studies have examined the efficacy of B. serrata in chronic pain conditions. The data suggest a clinical analgesic efficacy, without, however, allowing conclusions about the underlying mechanisms. These have not yet been investigated in a human experimental pain model. The aim of the study is to investigate the influence of Boswellia serrata in peripheral and central sensitization, as well as descending inhibitory pathways by Quantitative Sensory Testing (QST). These findings are of great relevance for a better understanding of clinical efficacy. The 'Capsaicin Pain Model' is a validated method for inducing short-term peripheral and central sensitization. As a non-invasive human pain model, it is therefore well suited for investigating the analgesic and anti-hyperalgesic effects of drugs. Furthermore, the influence of Boswellia serrata on mood (depression, anxiety), sleep quality and psychological well-being will be investigated by using the psychological questionnaires Becks-Depression-Inventory, Becks-Anxiety-Inventory, Pittsburgh Sleep Quality Index and World Health Organization Well-Being Index (BDI-II, BAI, PSQI and WHO5) as secondary target variables.

Participants needed: 12
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Medical University of GrazUpdated: Sep 24, 2025Locations: 1
Eligibility criteria

Age: ≥18 years

Not pregnant or breastfeeding [+9]

Status: Recruiting

Relationship Between Central Sensitization Symptoms and Cognitive Dysfunction in Fibromyalgia

The aim of the study is to investigate the relationship between central sensitization parameters and cognitive dysfunction in patients with fibromyalgia.The main questions it aims to answer are: Do central sensitization symptoms affect cognitive dysfunction in patients with fibromyalgia? To what extent do central sensitization symptoms affect objective and subjective cognitive complaints in fibromyalgia patients? How do cognitive complaints relate to other clinical parameters, including disease severity, in these patients?

Participants needed: 100
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Sultan Abdulhamid Han Training and Research Hospital, Istanbul, TurkeyUpdated: Sep 12, 2025Locations: 1
Eligibility criteria

Being diagnosed with fibromyalgia according to American College of Rheumatology... [+3]

Concomitant systemic inflammatory disease, central nervous system disease (corti... [+4]

Status: Recruiting

Investigation of the Relationship Between Central Sensitization and Balance in Fibromyalgia

The aim of the study is to investigate the relationship between central sensitization parameters and changes in static and dynamic balance in patients with fibromyalgia. The main questions it aims to answer are: * Do central sensitization parameters differ in patients with fibromyalgia compared to healthy individuals? * How is balance performance in these individuals compared to healthy controls? * Do central sensitization parameters affect static and dynamic balance in patients with fibromyalgia? * Do central sensitization parameters lead to quantitative changes in balance in patients with fibromyalgia?

Participants needed: 75
Trial details
Age: 18-65Biological sex: FemaleType: ObservationalSponsor: Sultan Abdulhamid Han Training and Research Hospital, Istanbul, TurkeyUpdated: Sep 12, 2025Locations: 1
Eligibility criteria

Diagnosis of FMS according to the ACR 2016 diagnostic criteria [+3]

Being under 18 years old or over 65 years old [+11]

Status: Recruiting

Investigation of Central Sensitization and Associated Factors in Patients With Lipedema

This study aims to investigate the presence of central sensitization and its associated parameters in patients with lipedema. Lipedema is a chronic and hereditary condition that primarily affects the lower extremities in women and is often associated with hormonal changes. Symptoms such as pain, swelling, and tenderness are common in lipedema, and these symptoms may be related to central sensitization. Additionally, the ultrasonographic findings and pain sensitivity in lipedema will be compared with those of healthy individuals. This study seeks to contribute to the diagnosis and treatment process of lipedema.

Participants needed: 50
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Sultan Abdulhamid Han Training and Research Hospital, Istanbul, TurkeyUpdated: Sep 8, 2025Locations: 1
Eligibility criteria

Lipedema; Diagnosis of lipedema Aged between 18 and 65 years Literate Willing to... [+1]

Lipedema group; Under 18 or over 65 years of age Presence of concurrent lymphede... [+1]

Status: Recruiting

Symptom Distribution and Pain Sensitization in Carpal Tunnel Syndrome

This study aims to compare central sensitization parameters between carpal tunnel syndrome (CTS) patients with extra median symptom distribution and those with typical, median nerve-related symptoms. Extra median sensory spread, observed in some CTS patients beyond the anatomical boundaries of the median nerve, may reflect central sensitization mechanisms. Using the Central Sensitization Inventory and pressure pain threshold measurements, this study will assess whether extra median symptom patterns are associated with increased central sensitization.

Participants needed: 80
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Sultan Abdulhamid Han Training and Research Hospital, Istanbul, TurkeyUpdated: Aug 11, 2025Locations: 1
Eligibility criteria

Having been diagnosed with carpal tunnel syndrome based on clinical and electrod... [+3]

Having a history of concomitant diabetes, systemic inflammatory disease, active... [+5]

Status: Recruiting

The Effect of Griffonia Simplicifolia on Pain Intensity, Central and Peripheral Sensitization, Painmodulation in Healthy Volunteers

This planned study is based on a randomized, placebo-controlled cross-over design. Griffonia simplicifolia contains the serotonin-precursor 5-hydroxytryptophan (5-HTP), an endogenous amino acid. 5-HTP can cross the blood-brain barrier and is converted to serotonin. Low serotonin levels are associated with depression, anxiety disorders and sleep disorders, among others. Griffonia simplicifolia is marketed as a food supplement in accordance with EU Directive 2002/46/EC. Several clinical studies have examined the efficacy of 5-HTP in chronic pain conditions. The data suggest a clinical analgesic efficacy, without, however, allowing conclusions about the underlying mechanisms. These have not yet been investigated in a human experimental pain model. The aim of the study is to investigate the influence of 5-HTP in peripheral and central sensitization, as well as descending inhibitory pathways by Quantitative Sensory Testing (QST). These findings are of great relevance for a better understanding of clinical efficacy. For this purpose, "repetitive phasic heat application" is a validated method for achieving short-term peripheral and central sensitization. As a non-invasive human pain model, it is therefore well suited for investigating the analgesic and anti-hyperalgesic effects of drugs. Furthermore, the influence of Griffonia simplicifolia on mood (depression, anxiety), memory, sleep quality and psychological well-being will be investigated by using psychological questionnaires as secondary target variables.

Participants needed: 20
Trial details
Age: 18-99Biological sex: AllType: InterventionalSponsor: Medical University of GrazUpdated: Jun 17, 2025Locations: 1
Eligibility criteria

pregnancy or breastfeeding. [+8]

Status: Recruiting

Evaluation of Central Sensitization, Fear-Avoidance, and Pain-Pressure Threshold With Chronic Pain After Hysterectomy

Phase 1 (started in July 2019): Central Sensitization Inventory (CSI), Fear-Avoidance Components Scale (FACS), pain-pressure threshold are factors associated with chronic post-hysterectomy pain (CPHP), but a complete understanding on the development of CPHP is lacking. The study aims to identify clinically-relevant factors for CPHP that can be reliably assessed preoperatively. === Phase 2 (anticipated start May 2022): In addition to above factors, the association between heart rate variability (HRV) parameters, anxiety level, anticipated pain, and anticipated analgesia requirement with significant postoperative pain and CPHP will be investigated.

Participants needed: 436
Trial details
Age: 21-80Biological sex: FemaleType: ObservationalSponsor: KK Women's and Children's HospitalUpdated: Nov 26, 2024Locations: 1
Eligibility criteria

Age 21 to 80 years old [+3]

Vaginal hysterectomy [+9]

Status: Recruiting

Myofascial Release Technique in Women With Primary Dysmenorrhea

It has been found that women with dysmenorrhea have active trigger points, particularly in the rectus abdominis, oblique abdominal muscles, quadratus lumborum, and paraspinal muscles. The myofascial release technique is a widely used manual therapy method characterized by the application of low-load, long-duration mechanical forces to manipulate the myofascial complex. This technique aims to restore optimal length, alleviate pain, and improve function. This study aims to examine the effect of the myofascial release technique on central sensitization, myofascial trigger points, and menstrual symptoms in women with primary dysmenorrhea.

Participants needed: 36
Trial details
Age: 18-35Biological sex: FemaleType: InterventionalSponsor: Gazi UniversityUpdated: Nov 21, 2024Locations: 1
Eligibility criteria

Diagnosed with Primary Dysmenorrhea according to the Primary Dysmenorrhea Consen... [+2]

Diagnosed with Secondary Dysmenorrhea, [+7]

Status: Not yet recruiting

Effect of Pregabalin on Shoulder Pain in Patients With Central Sensitization After Arthroscopic Rotator Cuff Repair

This study aims to investigate the effects of Pregabalin intake on shoulder pain management in patients with central sensitization undergoing arthroscopic rotator cuff repair. Although Pregabalin is known to be effective in controlling pain after shoulder arthroscopy, research on its efficacy in pain management for patients with central sensitization is scarce. Utilizing a list that identifies central sensitization, this study will explore whether Pregabalin can reduce postoperative pain in these patients and potentially improve joint mobility, emotional, and physical functioning. A prospective randomized study is planned, with inclusion criteria set for patients aged between 19 and 70 who have undergone arthroscopic rotator cuff repair. The study will compare clinical outcomes up to one year postoperatively between two groups of 38 patients each. The case group will receive standard postoperative medications (NSAIDs) plus Pregabalin oral intake from the day before surgery to six weeks postoperatively, while the control group will receive only the standard postoperative medications without Pregabalin.

Participants needed: 76
Trial details
Phase: Phase 4Age: 20-69Biological sex: AllType: InterventionalSponsor: The Catholic University of KoreaUpdated: Aug 23, 2024
Eligibility criteria

Age over 19 to under 70 [+3]

Previous history of Pregabalin prescription [+6]

Status: Not yet recruiting

Evaluation of the Effect of Central Sensitivity on Pain and Functional Status After Total Knee Joint Replacement Surgery

The study is a prospective observational study designed to determine the effects of central sensitization on pain and functional status of patients before and after total knee joint replacement surgery. The aim of this study is to evaluate whether there is a difference in preoperative and postoperative pain and functional status between patients with and without central sensitization with knee osteoarthritis. When the literature was reviewed, it was seen that central sensitization was one of the important mechanisms that caused pain in knee osteoarthritis, and it was determined that this had negative consequences in terms of postoperative pain and improvement in functional status. In this study, the effect of central sensitization on the results will be investigated by evaluating pain and functional status before and after knee total joint prosthesis in two groups of knee osteoarthritis patients, with and without central sensitization, and by comparing the groups.

Participants needed: 80
Trial details
Age: 60-75Biological sex: AllType: ObservationalSponsor: Istanbul UniversityUpdated: Aug 15, 2024
Eligibility criteria

Diagnosis of primary knee osteoarthritis [+2]

Having secondary knee osteoarthritis [+4]

Status: Not yet recruiting

Investigating the Association Between Central Sensitization and Breathing Pattern Disorders

Breathing pattern disorders can cause mechanical, physiological, and psychological issues in the body, contributing to the initiation and chronicity of pain. Therefore, considering breathing patterns is significant in managing chronic pain, yet direct research on central sensitization and breathing pattern disorders remains scant. This study aims to analyze the correlation between central sensitization and breathing pattern disorders in adults by assessing both respiration and pain.

Participants needed: 40
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Sahmyook UniversityUpdated: Jul 3, 2024Locations: 1
Eligibility criteria

Adults aged 18 and above. [+2]

Individuals with pulmonary, cardiac, or respiratory diseases. [+3]