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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 is a NA study that has completed, run by Atlantic Health System. The registered enrollment target is 88 participants.
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.
Interventions
- OTHER No Foley
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 88 participants |
| Start Date | 2015-12 |
| Est. Completion | 2017-09-21 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02765893
The ClinicalTrials.gov registry entry for NCT02765893 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 88 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Atlantic Health System, which has 43 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which No Foley is the first listed.
NCT02765893 reports 0 study locations.
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.
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