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

Launched by INOVA HEALTH CARE SERVICES · Feb 14, 2024

Keywords

ClinConnect Summary

This clinical trial is studying two different techniques for performing a surgical procedure called salpingectomy, which is a method of permanent sterilization, during a cesarean delivery (C-section). The trial aims to compare the outcomes and costs of using a hand-held device that uses heat (bipolar energy) versus the traditional method that uses stitches to close the fallopian tubes. Researchers want to find out if one technique works better than the other in the short term.

To participate in this study, women must be at least 21 years old, be 24 weeks pregnant or more, and request permanent sterilization during their C-section. They should also meet specific health requirements, such as not having had certain prior surgeries or specific pregnancy complications. If eligible, participants can expect to have their surgical outcomes monitored, and their experiences will contribute to understanding which method might be more effective and cost-efficient for sterilization during C-sections.

Gender

FEMALE

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.