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

Completed · Not applicable

Conditions studied: Sterility, Female

In brief

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.

Key facts

Study ID

NCT05518175

Run by

The University of Texas Health Science Center, Houston

People needed

255

Starts

2022-11-15

Expected to finish

2025-06-05

Last updated by the study team

2026-01-26

Who can join

Age: 18 and older, up to 55. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

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

You may not qualify if…

• 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

Where it is running

• The University of Texas Health Science Center at Houston — Houston, Texas, United States

Full record on ClinicalTrials.gov

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