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:
- Women who are seen at the DFEA department of the HUG (a hospital clinic) and have been prescribed the medication Ryeqo® by their doctor for an approved medical condition
- Women aged 18 years or older
Who may not be able to join:
- Women who are not able to speak and/or read French
- Women who have used certain hormonal medications in the past 3 months, including combined hormone pills (taken by mouth, worn as a patch, or used as a vaginal ring), estrogen tablets taken by mouth, or specific injectable or oral hormonal treatments (DMPA or nomegestrol acetate)
- Women who have not agreed to take part in the study
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: Patrick Petignat, Prof, University Hospital, Geneva
Phone: +41 79 55 35 385
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 from baseline in the mean value of normalized activated protein C resistance (nAPCsr) at 3 months of treatment with Ryeqo
Can't join this trial?
Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.