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11 clinical studies listed.

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Endometriosis-related Pain

Tundra lists 11 Endometriosis-related Pain clinical trials. Each listing includes eligibility criteria, study locations, and direct links to research sites in the Tundra directory.

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NOT YET RECRUITING

NCT07517081

Intraoperative Sono-assessment In Deep Endometriosis

Deep infiltrating endometriosis (DIE) involving the bowel, particularly the rectosigmoid region, is associated with significant gastrointestinal symptoms and impaired quality of life. Rectal shaving is a conservative surgical technique aimed at removing endometriotic lesions while preserving bowel integrity; however, it may result in residual disease or excessive thinning of the bowel wall, potentially leading to recurrence or complications. Intraoperative ultrasound (IOUS) allows real-time assessment of residual nodule thickness and bowel wall thickness after shaving. This prospective observational study aims to evaluate the relationship between intraoperative ultrasound measurements and postoperative clinical outcomes, including gastrointestinal symptoms and quality of life. The study also seeks to identify ultrasound cut-off values that may guide intraoperative surgical decision-making and optimize the balance between radicality and safety.

Gender: FEMALE

Ages: 20 Years - 60 Years

Updated: 2026-04-08

Endometriosis
Endometriosis-related Pain
Pelvic Pain Syndrome
+2
RECRUITING

NCT06795243

Efficacy of Physical Therapy Treatment in Endometriosis and Its Relationship to Adherence Rates.

The main objective of this study is to know if the application of both therapies, neuroscience pain education plus therapeutic exercise will modify pain, catastrophizing and quality of life in endometriosis.

Gender: FEMALE

Ages: 18 Years - Any

Updated: 2026-04-06

Endometriosis
Endometriosis Related Pain
Endometriosis, Pain
+11
NOT YET RECRUITING

NCT07440043

Relugolix for Endometriosis Associated Pain

Endometriosis is a chronic, estrogen-dependent condition frequently associated with pelvic pain and reduced quality of life. Relugolix combination therapy (CT), an oral GnRH receptor antagonist-based treatment, has demonstrated efficacy in randomized clinical trials, but real-world data remain limited. The RELAX study is a single-center, ambispective observational study evaluating the effectiveness of relugolix CT in reducing endometriosis-associated pain over 24 weeks in routine clinical practice. The primary endpoint is the change from baseline in pelvic pain measured by the Visual Analog Scale (VAS). Secondary outcomes include changes in pain-related symptoms, ultrasonographic findings, patient satisfaction, and safety.

Gender: FEMALE

Ages: 18 Years - 50 Years

Updated: 2026-02-27

Endometriosis
Endometriosis-related Pain
Pelvic Pain Syndrome
RECRUITING

NCT05754190

Assessing Symptom and Mood Dynamics in Pain Using the Smartphone Application SOMA

This study relies on the use of a smartphone application (SOMA) that the investigators developed for tracking daily mood, pain, and activity status in acute pain, chronic pain, and healthy controls over four months.The primary goal of the study is to use fluctuations in daily self-reported symptoms to identify computational predictors of acute-chronic pain transition, pain recovery, and/or chronic pain maintenance or flareups. The general study will include anyone with current acute or chronic pain, while a smaller sub-study will use a subset of patients from the chronic pain group who have been diagnosed with chronic low back pain, failed back surgery syndrome, or fibromyalgia. These sub-study participants will first take part in one in-person EEG testing session while completing simple interoception and reinforcement learning tasks and then begin daily use of the SOMA app. Electrophysiologic and behavioral data from the EEG testing session will be used to determine predictors of treatment response in the sub-study.

Gender: All

Ages: 18 Years - Any

Updated: 2025-09-19

1 state

Chronic Pain
Acute Pain
Post Operative Pain
+20
RECRUITING

NCT06579040

The HEROES Trial: Hyperbaric Oxygen Therapy for Endometriosis-Related Pain

Endometriosis, is a condition where tissue from the uterus, called endometrium, grows outside of the uterus. This effects up to 10% of women, and can lead to long-lasting, moderate to severe pelvic pain, infertility and other symptoms. This can affect a woman's quality of life (including increased risk of depression and anxiety) and is associated with increased healthcare costs. Current treatments are often limited by serious side effects, and many women resort to surgery. Surgery is also associated with complications and there are long wait times for procedures, sometimes over 3 years. This means that many women continue to suffer from symptoms while they wait for surgery. Therefore, new effective treatments for endometriosis pain are needed. New research suggests that inflammation and stress caused by lack of oxygen in the affected areas may cause endometriosis. Hyperbaric Oxygen Therapy (HBOT), where patients are placed in a small chamber with higher than normal levels of oxygen, suppresses inflammation and promotes tissue healing. Because inflammation is central to this condition, HBOT has emerged as a potential treatment. In this study, the investigators will test if HBOT, in addition to the standard treatments, is more effective at treating endometriosis pain than the standard treatments alone.

Gender: All

Ages: 18 Years - Any

Updated: 2025-09-09

1 state

Endometriosis-related Pain
RECRUITING

NCT06963177

A Phase IIa Clinical Study to Assess the Efficacy and Safety of GenSci048 in Patients With Moderate to Severe Endometriosis-Associated Pain

This study is designed to evaluate the safety and efficacy of GenSci048 for moderate to severe endometriosis-associated pain treatment.

Gender: FEMALE

Ages: 18 Years - 49 Years

Updated: 2025-08-12

1 state

Endometriosis-related Pain
RECRUITING

NCT05152264

Transcutaneous Electrical Nerve Stimulation for Endometriosis-related Chronic Pain

The study evaluates the effect of TENS (transcutaneous electrical nerve stimulation) as add-on treatment compared with conventional analgesic treatment in patients with endometriosis-related chronic pain. Patients with frequent pain and high pain intensity will be randomized to additional treatment with TENS or conventional treatment for 8 weeks to evaluate the acute effects of TENS treatment (n=40). Patients with endometriosis-related pain that is not frequent or without high pain intensity constitute an external control group. All patients in the study will receive TENS treatment for a total of 16 weeks, for evaluation of long-term effects of TENS treatment.

Gender: FEMALE

Ages: 18 Years - 100 Years

Updated: 2025-05-23

Endometriosis-related Pain
RECRUITING

NCT05978414

Functional Links Between the Temporomandibular Joint and the Pelvis in Gynecology

1 Recruitment. 2. Collection of written consents for the study. 3. Random assignment to groups with and without intervention. 4. Completion of questionnaires by study participants, postural pattern assessment, temporomandibular joint assessment, and platform assessment. 5\. Performance of visceral therapy in the group with intervention, in the group without intervention placebo. Duration 5 weeks, treatment 1x per week at the same time of day and given day e.g. Mondays only. 6\. Reassessment as in step 4. 7. Data collection, statistical analyses. 8. Interpretation of results for female participants. 9. Preparation of results for scientific publications.

Gender: FEMALE

Ages: 18 Years - 60 Years

Updated: 2025-02-07

Prolapse; Female
Endometriosis-related Pain
ACTIVE NOT RECRUITING

NCT04554693

The Use of Low Dose Metronidazole to Decrease Postoperative Pain After Endometriosis Surgery

The purpose of this study is to determine a difference in participant reported pain after endometriosis surgery in participants given oral metronidazole versus placebo.

Gender: FEMALE

Ages: 18 Years - 50 Years

Updated: 2025-01-27

1 state

Endometriosis
Endometriosis-related Pain
ACTIVE NOT RECRUITING

NCT04204707

Patient Reported Outcomes After Surgery for Rectal Endometriosis

To describe the difference in patient reported outcomes after conservative treatment in comparison to radical rectal surgery in patients with deep endometriosis infiltrating the rectum (up to 15cm from the anus with at least involvement of the muscularis layer) and to determine predictors for radical surgery.

Gender: FEMALE

Ages: 18 Years - 45 Years

Updated: 2024-12-10

Endometriosis
Endometriosis, Rectum
Endometriosis-related Pain
+1
RECRUITING

NCT06414083

Histologic Comparison of Ablative Techniques for Endometriosis

To our knowledge, no other human studies directly compare the effectiveness of the various ablative technologies. We set out to design a study to directly compare ablative energy sources and evaluate their ability to destroy native endometriosis tissue in humans.

Gender: FEMALE

Ages: 18 Years - Any

Updated: 2024-05-30

1 state

Endometriosis
Endometriosis-related Pain
Endometriosis Pelvic
+1