Endometriosis Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- You are a woman aged 18 or older
- You have been diagnosed with endometriosis and/or adenomyosis through a scan or tissue test
- You have been on the same hormone treatment (which has stopped your periods) continuously for at least 2 months
- You are not planning to change your hormone treatment during the study
- You have had ongoing pelvic pain for more than 6 months
- Your pelvic pain is at least "moderate" on a scale from none to severe
- You are willing to take part in the study
- You agree to only use certain approved pain relief medications during the study (paracetamol, Acupan®, and Antadys®)
- You have access to a computer, tablet, or mobile phone with an internet connection
- You are covered by a social security or health insurance system
Who may not be able to join:
- You are pregnant or breastfeeding
- You have gone through menopause
- Your endometriosis symptoms have gotten significantly worse in the last 28 days (confirm with trial site)
- You have reduced skin sensitivity in the area where the study device would be applied
- You have a known skin allergy to gel or electrode pads
- You have a skin condition in the area where the device would be placed
- You have a pacemaker or other active implanted medical device
- You have epilepsy
- You currently have a blood clot condition (thrombophlebitis or arterial thrombosis)
- You have cancer with a life expectancy of less than 12 months
- You have issues with alcohol or drug addiction
- You have fibromyalgia
- You have previously tried TENS therapy (a type of electrical nerve stimulation for pain)
- You are not able to communicate fluently in English
- You have cognitive impairments that affect understanding or memory
- You have a severe, untreated psychiatric or psychological condition that is considered the main cause of your symptoms
- You are currently taking part in another intervention study that could affect the results of this one
- You have been taking high doses of opioid-based painkillers (more than 90 morphine equivalents per day) at least once in the last 28 days
- You have gynaecological or endometriosis surgery planned in the next 3 months
- You have had endometriosis surgery within the last 6 months
- You have had your uterus removed (hysterectomy) or both ovaries removed (bilateral oophorectomy)
- You are under legal guardianship or have had your personal freedoms restricted by law
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Bejamin MERLOT, IFEM Endo, Clinique Tivoli-Ducos, 5 rue Auguste Poirson, 33000 Bordeaux, France
Phone: +33-389497361
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Change in the mean value of average pain
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.