NCT05820139View on ClinicalTrials.gov

Evaluating the Optimal Volume Voided for Passage of a Backfill-Assisted Voiding Trial Following Urogynecologic Surgery

NACompletedINTERVENTIONAL
Enrollment

100

Participants

Timeline

Start Date

July 11, 2023

Primary Completion Date

February 26, 2024

Study Completion Date

February 26, 2024

Conditions
Voiding Dysfunction
Interventions
PROCEDURE

Control Group

Patients will be randomized to a 200mL (control group)

PROCEDURE

Test Group

Patients will be randomized to a cut-off of 150mL (test group)

Trial Locations (1)

27157

Wake Forest University Health Sciences, Winston-Salem

All Listed Sponsors
lead

Wake Forest University Health Sciences

OTHER