Clin2
NCT07030426Likely a fitRecruiting

Vaginal estrogen before and after prolapse surgery

Pelvic Organ Prolapse (POP)

Part of Women’s health & pregnancy clinical trials.

This trial tests whether using vaginal estrogen before and after prolapse surgery helps improve recovery and long-term results. Women having apical suspension surgery (to support the top of the vagina) may benefit.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 3
Enrollment
180 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You are 18 years or older.
  • You are planning surgery to repair pelvic organ prolapse that supports the top of the vagina (apical suspension), either through the vagina or abdomen.
  • You have not had mesh placed for prolapse in a previous surgery.
  • You are willing to complete surveys about your pelvic health, sexual health, and function before and after surgery.
  • You plan to stay in the study area for at least 2 years after your surgery.
  • You do not have conditions that prevent using vaginal estrogen, such as breast cancer, unexplained bleeding, liver problems, blood clots, or a history of stroke or heart attack.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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