Clin2
NCT07625852Likely a fitNot yet recruiting

Comparing two surgical techniques for uterine scar defects

Isthmocele

Part of Women’s health & pregnancy clinical trials.

This study compares two different ways of closing a surgical defect in the uterus (called an isthmocele) that develops after a cesarean section. The trial tests whether one closure technique produces better outcomes than the other for women experiencing symptoms like abnormal bleeding, pelvic pain, or difficulty getting pregnant.

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

Phase
N/A
Enrollment
72 people
Ages
18 years to 45 years
Study type
Interventional

Who can take part

  • You are a woman aged 18–45 years old
  • You have had at least one prior cesarean section (C-section)
  • You have been diagnosed with an isthmocele (a defect in the uterine wall confirmed by ultrasound)
  • You are experiencing symptoms from the isthmocele, such as abnormal bleeding, pelvic pain, painful periods, or trouble conceiving
  • You are not currently pregnant
  • You are willing and able to attend follow-up appointments after surgery

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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