Clinical trial Recruiting at 1 site Phase 3 Interventional Ages 18 to 40 Women only

Effect of GnRH Agonist on Endometriosis Cysts

Official title: Effect of GnRH Agonist Administration on Decreasing VAS, Estradiol, and Anti Mullerian Hormone in Endometriosis Cyst Patients

Run by Rumah Sakit Pusat Angkatan Darat Gatot Soebroto · NCT06525155 · Data updated 2026-11-12

This study tests if a new medication can help women aged 18 to 40 with endometriosis cysts feel less pain and have fewer side effects before and after surgery.

Quick facts

PhasePhase 3
Study typeInterventional
Ages18 Years to 40 Years
SexWomen only
Enrollment32 (estimated)
SponsorRumah Sakit Pusat Angkatan Darat Gatot Soebroto
Academic / other
Locations1 site (Jakarta)
StatusRecruiting
StartedJanuary 2, 2024
Main results expectedFebruary 2025
Study endsFebruary 2025
Registry record updatedNovember 25, 2024
Trial IDNCT06525155 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are females aged 18 to 40 diagnosed with endometriosis cysts who have regular menstrual cycles.

Probably not a fit

Patients who have used hormonal contraception or GnRH agonists in the last three months, or those with certain medical histories, may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This clinical trial investigates the effectiveness of triptorelin embonate, a GnRH agonist, in treating endometriosis cysts in women aged 18 to 40. Participants will be divided into two groups, receiving either two doses before surgery and one after, or just one dose after surgery. The study will evaluate pain relief using a visual analogue scale and measure hormone levels at specified intervals. The goal is to determine if a longer dosing interval can improve patient compliance and reduce side effects.

Why it matters

Potential benefit: If successful, this treatment could provide a more effective and patient-friendly approach to managing endometriosis symptoms.

How similar studies have gone: Previous studies have indicated that extended dosing intervals of triptorelin may be effective, suggesting potential success for this approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Female subjects aged 18 to 40 years.
* The subjects was diagnosed with endometriosis cysts.
* Willing to participate in research and sign informed consent before all research-related activities begin.
* Regular menstruation (within 25 - 35 day intervals) in the last 3 months before the study was conducted.

Exclusion Criteria:

* The patient used hormonal contraception in the last 3 months prior to the study.
* Using a GnRH agonist within the past 3 months.
* Using the hormone progesterone within the last 3 months
* Pregnancy, breastfeeding females
* History of osteoporosis
* History of blood clotting disorders
* History of heart and blood vessel disorders

Where it's running

  • Department of Obstetrics and Gynecology Central Army Hospital Gatot Soebroto
    Jakarta, Indonesia
    Recruiting

Study contacts

  • Principal investigator: Surya A Pramono, Sp.OG., Subsp.FER, MD — Rumah Sakit Pusat Angkatan Darat Gatot Soebroto
  • Study coordinator: Surya A Pramono, Sp.OG., Subsp.FER, MD
  • Email: suryaadipramono230781@gmail.com
  • Phone: +6282145122104

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
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Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.