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NCT02765893 · ClinicalTrials.gov registry record · NA
Indwelling vs Immediate Removal of Foley Catheter After Robotic Assisted Laparoscopic Sacrocolpopexy: a Prospective Study
A NA study, sponsored by Atlantic Health System.
- Completed
- Registry status
- NA
- Development phase
- 88
- Enrollment target
NCT02765893: Completed NA study, sponsored by Atlantic Health System.
NCT02765893 is a NA study that has completed, run by Atlantic Health System. The registered enrollment target is 88 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (94% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02765893, a NA study, has completed, sponsored by Atlantic Health System.
- COMPLETED
- Registry status
- NA
- Development phase
- 88 participants
- Enrollment target
Study 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.
Primary Outcome
Patients in the intervention group will have their Foley catheter removed up to 6 hours after discharge from the PCA. They will then have to undergo a voiding trial
Interventions
- OTHER No Foley
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 88 participants |
| Start Date | 2015-12 |
| Est. Completion | 2017-09-21 |
| Phase | NA |
What the finished NCT02765893 record still lists
NCT02765893 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 88 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (94% lower).
The record links to 0 conditions, and to 1 intervention - of which No Foley is the first listed.
NCT02765893 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02765893 about?
NCT02765893 is a clinical study titled "Indwelling vs Immediate Removal of Foley Catheter After Robotic Assisted Laparoscopic Sacrocolpopexy: a Prospective Study". 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 gro...
What is the current status of trial NCT02765893?
This trial is currently completed. It is a NA study. The enrollment target is 88 participants. The study started on 2015-12. Estimated completion is 2017-09-21.
What interventions are being tested in trial NCT02765893?
The interventions under investigation include: No Foley (OTHER).
Who is sponsoring clinical trial NCT02765893?
This trial is sponsored by Atlantic Health System, which has 43 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02765893's enrollment target sits among peer trials
88 972nd of 2000 higher than 1,027 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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