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

Last updated: April 25, 2023
Sponsor: The University of Texas Health Science Center, Houston
Overall Status: Active - Recruiting

Phase

N/A

Condition

Infertility

Treatment

N/A

Clinical Study ID

NCT05518175
HSC-MS-22-0470
  • Ages 18-55
  • Female

Study Summary

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 Criteria

Inclusion

Inclusion Criteria:

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

Exclusion

Exclusion Criteria:

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

Study Design

Total Participants: 150
Study Start date:
November 15, 2022
Estimated Completion Date:
December 31, 2024

Connect with a study center

  • The University of Texas Health Science Center at Houston

    Houston, Texas 77030
    United States

    Active - Recruiting

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