Status:
COMPLETED
The Impact of a Redesigned Handout for Robotic Sacrocolpopexy on Patient Preoperative Preparedness and Satisfaction
Lead Sponsor:
University of Texas Southwestern Medical Center
Collaborating Sponsors:
University of Texas, Southwestern Medical Center at Dallas
Conditions:
Pelvic Organ Prolapse
Patient Satisfaction
Eligibility:
FEMALE
18+ years
Phase:
NA
Brief Summary
The goal of this clinical trial is to learn if a new preoperative handout for patients undergoing robotic sacrocolpopexy will improve patient sense of preparedness and satisfaction in comparison to th...
Eligibility Criteria
Inclusion
- women who were to undergo robotic sacrocolpopexy with or without supracervical hysterectomy, rectopexy, salpingectomy, urinary incontinence procedures, or other minor procedures.
Exclusion
- patients unable to provide informed consent, those undergoing other concomitant major abdominal surgeries, patients less than 18 years old, pregnant patients, non-English speaking patients, and patients planning postoperative follow up at an outside facility.
Key Trial Info
Start Date :
August 1 2022
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 31 2023
Estimated Enrollment :
51 Patients enrolled
Trial Details
Trial ID
NCT06934304
Start Date
August 1 2022
End Date
December 31 2023
Last Update
April 18 2025
Active Locations (1)
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1
University of Texas Southwestern Medical Center
Dallas, Texas, United States, 75390