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
| Type | Name | Description |
|---|---|---|
| OTHER | No Foley | Patients 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.