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Patient-centered Outcomes After Permanent Female Sterilization Procedure(POPS Trial)

Recruiting
18 - 55 years of age
Female
Phase N/A

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Overview

The purpose of this study is to compare and capture key elements of the patient experience, quality of recovery, preferences and satisfaction after laparoscopic salpingectomy done via 3 different routes.

Eligibility

Inclusion Criteria:

  • Premenopausal women scheduled to undergo an elective sterilization surgery regardless of parity
  • non-prolapsed uterus
  • Patients should able to provide written consent

Exclusion Criteria:

  • Women who have relative contra-indication to vaginal peritoneal access such as: history of rectal surgery, suspected recto-vaginal endometriosis based on clinical history and examination, suspected malignancy, pelvic inflammatory disease, active lower genital tract infection, virginity or pregnancy
  • Postpartum (immediate) tubal sterilization
  • Tubal sterilization during a cesarean section

Study details

Sterility, Female

NCT05518175

The University of Texas Health Science Center, Houston

27 January 2024

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