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NCT03992079 · ClinicalTrials.gov registry record · NA
A Multimodal Enhanced Recovery Program in Anorectal Surgery
A NA study, sponsored by Columbia University.
- Terminated
- Registry status
- NA
- Development phase
- 60
- Enrollment target
NCT03992079 is a NA study that was terminated before completion, run by Columbia University. The registered enrollment target is 60 participants.
The verdict
NCT03992079, a NA study, was terminated before completion, sponsored by Columbia University.
- TERMINATED
- Registry status
- NA
- Development phase
- 60 participants
- Enrollment target
Study Summary
The goal of this study is to establish whether an opioid-sparing Enhanced Recovery After Surgery (ERAS) program in ambulatory anorectal surgery can be safely introduced at a single tertiary referral center without an increase in postoperative pain or negative impact on the patient experience. A single-center, single-blinded randomized control trial is proposed, where patients will be assigned in a 1:1 ratio to either usual care, which includes extended opioids (control group) or the enhanced recovery group (experimental), which includes preemptive pain control, targeted education, and multimodal opioid-sparing pain management during the intraoperative and postoperative periods. The expected outcome is that the enhanced recovery program will significantly reduce opioid utilization with comparable pain scores and patient satisfaction after anorectal surgery.
Interventions
- PROCEDURE ReCOVER Enhanced Recovery Protocol
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 60 participants |
| Start Date | 2019-06-20 |
| Est. Completion | 2020-05-21 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03992079
The ClinicalTrials.gov registry entry for NCT03992079 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Columbia University, which has 958 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which ReCOVER Enhanced Recovery Protocol is the first listed.
NCT03992079 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT03992079 about?
NCT03992079 is a clinical study titled "A Multimodal Enhanced Recovery Program in Anorectal Surgery". The goal of this study is to establish whether an opioid-sparing Enhanced Recovery After Surgery (ERAS) program in ambulatory anorectal surgery can be safely introduced at a single tertiary referral center without an increase in postoperative pain or negative impact on the patient experience. A sing...
What is the current status of trial NCT03992079?
This trial is currently terminated. It is a NA study. The enrollment target is 60 participants. The study started on 2019-06-20. Estimated completion is 2020-05-21.
What interventions are being tested in trial NCT03992079?
The interventions under investigation include: ReCOVER Enhanced Recovery Protocol (PROCEDURE).
Who is sponsoring clinical trial NCT03992079?
This trial is sponsored by Columbia University, which has 958 total clinical trials registered on ClinicalTrials.gov.
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