Finished
Indwelling vs Immediate Removal of Foley Catheter After Robotic Assisted Laparoscopic Sacrocolpopexy: a Prospective Study
NCT02765893 · Atlantic Health System · Updated 25 Oct 2017
- What is being tested
- No Foley
- For
- Urinary Retention
- Kind of study
- Tests a treatment or device on volunteers. No drug phase (a device or procedure study).
- Who can join
- Ages 19 years to 75 years. About 88 people. The full rules are on the registry page.
- Where
- United States
- When
- Starts or started Dec 2015, ends 21 Sept 2017. Registered 9 May 2016.
- Results
- None posted yet.
In the researchers' words
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.
Sites
- Atlantic HealthMorristown, New Jersey, United States
