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NCT07686783Recruiting

Ovarian Reserve After Laparoscopic Cystectomy for Endometriotic and Non-Endometriotic Cysts

Ovarian Reserve After Laparoscopic Cystectomy for Endometriotic and Non-Endometriotic Cysts: A Comparative Prospective Cohort Study

Source: ClinicalTrials.gov · Last updated 30 Sept 2026

Brief summary (registry, in English)

We will conduct this study to estimate the effect of laparoscopic cystectomy on ovarian reserve in endometriotic cysts versus non-endometriotic cysts.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
60 (estimated)
First submitted
27 Jun 2026
Start date
30 Jun 2026
Primary completion date
30 Jun 2027
Lead sponsor
Benha University
NCT number
NCT07686783

What you commit to

  • Study type: Interventional
  • Planned participants: 60
  • From 30 Jun 2026 to the primary completion date, 30 Jun 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previous history of ovarian surgery
  • Current use of hormonal contraceptives or hormonal therapy within 3 months prior to enrollment

Other illness

  • Clinical or ultrasonic suspicion of ovarian malignancy
  • History of pelvic irradiation or chemotherapy
  • Known endocrine disorders affecting ovarian function (e.g., PCOS, premature ovarian insufficiency, thyroid dysfunction, hyperprolactinemia)
  • Presence of severe systemic disease that contraindicates surgery or general anesthesia

Other

  • Ovarian cyst associated with pregnancy
  • Refusal to participate or inability to provide informed consent

Who the study is looking for

  • Female patients aged 18-45 years
  • Ovarian cyst measuring 6-15 cm in diameter, confirmed by transvaginal ultrasound or MRI
  • Cyst is persistent for more than 3 months if asymptomatic, OR any symptomatic cyst regardless of duration of diagnosis
  • Serum anti-Müllerian hormone (AMH) level ≥ 2 ng/mL, measured within 1 month preoperatively
  • Willingness to participate and provide written informed consent

Age in the registry: 18 years to 45 years · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Benha Univesity Hospital
Coordinator of this site? Confirm its status
BanhāEgyptRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.