At a glance
ClinicalIndex Comparison RecordN/ACompleted· 88 enrolled
Drug / intervention
No Foleyother
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Indwelling vs Immediate Removal of Foley Catheter After Robotic Assisted Laparoscopic Sacrocolpopexy: a Prospective Study
In Brief
A clinical study evaluating No Foley for Urinary Retention. Completed, enrolled 88 participants across 1 site.
Detailed Summary
This is a prospective, comparative randomized study. Our study population includes women with pelvic organ prolapse undergoing a robotic assisted laparoscopic sacrocolpopexy. The two groups will include the study group, who will have their Foley catheter removed 6 hours post-op, and the control group who will have an indwelling Foley catheter overnight. The two groups will be assigned according REDCap randomization system.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsUrinary Retention
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
20162017201820192020202120222023202420252026
Enrollment StartDec 2015
First PostedMay 2016
Primary CompletionSep 2017
TodayJul 2026
First PostedMay 9, 2016
Enrollment StartDec 1, 2015
Primary CompletionSep 21, 2017
TodayJul 2, 2026
Enrollment to primary: 1.8 yearsPosted 10.1 years ago
Interventions
No Foleyother
Patients will have Foley catheter removed 6 hours post-op.