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NCT07519213Completed

Guangdong Endometriosis Retrospective Clinical Cohort

Guangdong Retrospective Clinical Cohort Study of Endometriosis

Source: ClinicalTrials.gov · Last updated 8 Jul 2026

Brief summary (registry, in English)

This retrospective cohort study evaluates the association between postoperative hormonal treatment and recurrence of ovarian endometriosis in women undergoing surgery for ovarian endometrioma. The study includes patients treated at a single center who initiated one postoperative hormonal regimen after surgery. The main objective is to compare the risk of recurrence among women receiving combined oral contraceptives, gonadotropin-releasing hormone agonists, dienogest, or dydrogesterone. Recurrence is assessed during follow-up based on postoperative clinical and ultrasound findings. The results may help clarify the comparative effectiveness of commonly used postoperative hormonal strategies for reducing recurrence after surgery for ovarian endometrioma.

Status (registry)
Completed
Study type
Observational
Enrollment
1121 (actual)
First submitted
2 Apr 2026
Start date
1 Sept 2025
Primary completion date
1 Jan 2026
Lead sponsor
Guangdong Women and Children Hospital
NCT number
NCT07519213

What you commit to

  • Study type: Observational
  • Participants enrolled: 1121
  • From 1 Sept 2025 to the primary completion date, 1 Jan 2026
  • 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

  • Use of sequential or multiple postoperative hormonal therapies during the initial treatment period.

Other illness

  • Failure to initiate postoperative hormonal therapy within 1 month after surgery.

Other

  • Discontinuation of the postoperative hormonal regimen before 6 months.
  • Incomplete clinical records or insufficient follow-up data for evaluation of recurrence.

Who the study is looking for

  • Female patients who underwent conservative surgery for ovarian endometrioma at the study center.
  • Initiation of one postoperative hormonal regimen within 1 month after surgery.
  • Continuous use of the same single hormonal regimen for at least 6 months after surgery.
  • Availability of clinical records and postoperative follow-up data for assessment of study outcomes.

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
Guangdong Women and Children Hospital
Coordinator of this site? Confirm its status
GuangzhouChinaUnknown status

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