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Recruiting NCT06273683

Comparison of Two Salpingectomy Techniques for Sterilization at the Time of Cesarean Delivery

Trial Parameters

Condition Permanent Sterilization
Sponsor Inova Health Care Services
Study Type OBSERVATIONAL
Phase N/A
Enrollment 900
Sex FEMALE
Min Age 21 Years
Max Age N/A
Start Date 2024-03-11
Completion 2027-12
Interventions
Hand-held bipolar energy instrumentTraditional suture ligation

Brief Summary

One in three women of reproductive age utilize tubal sterilization for contraception, and sterilization is often requested at time of cesarean delivery. Complete salpingectomy for the purpose of permanent sterilization at the time of cesarean birth is increasingly being performed worldwide. A preferred complete salpingectomy technique for the purpose of sterilization at the time of cesarean delivery has not emerged in current practice. The objective is to compare short-term clinical outcomes and cost of salpingectomy using a hand-held bipolar energy instrument with those of traditional suture ligation. This retrospective cohort study will be conducted from 2017-2023 at a single tertiary care hospital. The investigators hypothesize that bipolar energy instrument use will not significantly improve clinical outcomes.

Eligibility Criteria

Inclusion Criteria: * request for permanent sterilization at the time of cesarean delivery * 24 weeks' gestation or beyond * 21 years old or older * Medicaid sterilization consent per Virginia Department of Medical Assistance Services regulations (if Medicaid recipient). Exclusion Criteria: * vaginal delivery * history of prior adnexal surgery (such as prior bilateral tubal ligation or unilateral salpingectomy oophorectomy) * placenta accreta spectrum * placenta previa * history of bleeding diathesis.

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