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Study identifier: NCT07065214 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Argon Plasma Treatment for Ovarian Endometrioma Compared to Standard Cystectomy

Condition: Endometriosis  ·  Sponsor: Erbe Elektromedizin GmbH

PhaseNA
Planned participants72
Who can joinFemale, 18 Years to 40 Years
Healthy volunteersNo

About this study

The study is a prospective, monocentric, randomized controlled, two-armed, pilot-study conducted at Department for Women's Health, Tuebingen, Germany. In this Post Market Study it will be determined whether and to what extent the two surgical procedures for ovarian endometrioma treatment (standard cystectomy versus APC) may affect the ovarian reserve by comparing changes in serum AMH levels after treatment. Seventy-two (72) patients who meet all eligibility criteria will undergo surgical procedure. The patients will be randomized into the group with standard cystectomy treatment or with APC treatment. Per group n=36 patients will be treated i.e., 1:1 randomization. A pre-specified primary endpoint analysis is planned after the last patient has undergo Visit 4 (Follow-up after 6 months) to analyze the primary endpoint. Screening takes place during the first visit (V1). During the second visit (V2) the participants will receive the ovarian endometriosis treatment procedure either with the APC or the standard cystectomy. Standard procedure (standard cystectomy) will be performed for additional endometriosis lesions. The follow up visits (V3 - V5) will take place after three, six and twelve months. Visit 3 and Visit 4 will take place at the study site and AMH will be measured. Whereas Visit 5 will take place via telemedical contact, i.e. phone call.

This description comes directly from the study's public registry record.

Talk to the study team

Vanessa Steinmetz  ·  +49 70717552850  ·  vanessa.steinmetz@erbe-med.com

Always discuss trial participation with your own doctor first.

Locations (1)

Department for Women's HealthTübingen, Germany, GermanyRecruiting

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Source record: clinicaltrials.gov/study/NCT07065214