Clinical Trials Directory

Trials / Completed

CompletedNCT02765893

Indwelling vs Immediate Removal of Foley Catheter After Robotic Assisted Laparoscopic Sacrocolpopexy: a Prospective Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
88 (actual)
Sponsor
Atlantic Health System · Academic / Other
Sex
Female
Age
19 Years – 75 Years
Healthy volunteers
Accepted

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.

Conditions

Interventions

TypeNameDescription
OTHERNo FoleyPatients will have Foley catheter removed 6 hours post-op.

Timeline

Start date
2015-12-01
Primary completion
2017-09-21
Completion
2017-09-21
First posted
2016-05-09
Last updated
2017-10-25

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02765893. Inclusion in this directory is not an endorsement.

Indwelling vs Immediate Removal of Foley Catheter After Robotic Assisted Laparoscopic Sacrocolpopexy: a Prospective Stud (NCT02765893) · Clinical Trials Directory