CompletedNot Applicable

Cohort Study of Risk Reducing Salpingectomy

United States18 participantsStarted 2014-06

Plain-language summary

Women undergoing surgical sterilization will be interested in risk reducing salpingectomy, and surgeons performing the procedure will be able to successfully complete the salpingectomy.

Who can participate

Age range35 Years – 60 Years

SexFEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Women \> 35 years requesting sterilization as interval procedure OR at time of cesarean delivery * At least one living child * English or Spanish speaking * Sterilization planned as interval (laparoscopic) procedure via Family Planning Clinic services or at time of delivery * Delivery by cesarean section (planned or following labor) Exclusion Criteria: * Age \< 30 * Medical complications that increase risk for surgical bleeding (e.g. Idiopathic thrombocytopenic purpura (ITP); von Willebrand disease (vWD); need for prophylactic or therapeutic anticoagulation)

What they're measuring

Percent of women accepting RRS

Timeframe: 12 months

Trial details

NCT IDNCT02165709

SponsorUniversity of North Carolina, Chapel Hill

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2015-08

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