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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.
ClinicalTrials.gov, NCT02765893

Sites

  • Atlantic HealthMorristown, New Jersey, United States