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NCT04197869 · ClinicalTrials.gov registry record · Phase 4
Does a Preoperative Bowel Regimen Change Time to First Bowel Movement After Robotic Sacral Colpopexy
A Phase 4 study, sponsored by Northwell Health.
- Completed
- Registry status
- Phase 4
- Development phase
- 71
- Enrollment target
NCT04197869 is a Phase 4 study that has completed, run by Northwell Health. The registered enrollment target is 71 participants.
The verdict
NCT04197869, a Phase 4 study, has completed, sponsored by Northwell Health.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 71 participants
- Enrollment target
Study Summary
The hypothesis is that starting a bowel regimen with Polyethylene Glycol prior to robotic assisted sacrocolpopexy will decrease time to first bowel movement after surgery. The experimental group will take a pre-operative course of polyethylene glycol daily for seven days prior to procedure date. The control group will not be given any intervention preoperatively. All patients will take polyethylene glycol postoperatively.
Interventions
- DRUG Polyethylene Glycol Powder
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 71 participants |
| Start Date | 2019-12-09 |
| Est. Completion | 2023-06-21 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04197869
The ClinicalTrials.gov registry entry for NCT04197869 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 71 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Northwell Health, which has 370 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Polyethylene Glycol Powder is the first listed.
NCT04197869 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT04197869 about?
NCT04197869 is a clinical study titled "Does a Preoperative Bowel Regimen Change Time to First Bowel Movement After Robotic Sacral Colpopexy". The hypothesis is that starting a bowel regimen with Polyethylene Glycol prior to robotic assisted sacrocolpopexy will decrease time to first bowel movement after surgery. The experimental group will take a pre-operative course of polyethylene glycol daily for seven days prior to procedure date. The...
What is the current status of trial NCT04197869?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 71 participants. The study started on 2019-12-09. Estimated completion is 2023-06-21.
What interventions are being tested in trial NCT04197869?
The interventions under investigation include: Polyethylene Glycol Powder (DRUG).
Who is sponsoring clinical trial NCT04197869?
This trial is sponsored by Northwell Health, which has 370 total clinical trials registered on ClinicalTrials.gov.
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