MedTrace Logo

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

NCT05518175 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 255

Last updated 2026-01-26

No results posted yet for this 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.

Conditions

  • Sterility, Female

Interventions

PROCEDURE

Traditional laparoscopy

Utilizes three or four ports for access and retrieval.

PROCEDURE

Single site laparoscopy

One port is placed via a 2 to 3 cm umbilical/fascia incision. With this technique, there is a single incision, hidden in the umbilicus.

PROCEDURE

V-Notes surgery

One port placed trans-vaginally via a 2-3 cm vaginal incision with no abdominal scars.

Sponsors & Collaborators

  • The University of Texas Health Science Center, Houston

    lead OTHER

Principal Investigators

  • Randa J Jalloul, MD · The University of Texas Health Science Center, Houston

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
55 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-11-15
Primary Completion
2025-03-07
Completion
2025-06-05

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05518175 on ClinicalTrials.gov