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NCT03684304 · ClinicalTrials.gov registry record · NA
The Effect of Abdominal Binder Use on Postoperative Pain and Mobility in Patients Undergoing Pelvic Surgery
A NA study, sponsored by University Hospitals Cleveland Medical Center.
- Terminated
- Registry status
- NA
- Development phase
- 36
- Enrollment target
NCT03684304 is a NA study that was terminated before completion, run by University Hospitals Cleveland Medical Center. The registered enrollment target is 36 participants.
The verdict
NCT03684304, a NA study, was terminated before completion, sponsored by University Hospitals Cleveland Medical Center.
- TERMINATED
- Registry status
- NA
- Development phase
- 36 participants
- Enrollment target
Study Summary
To determine the effect of post-operative abdominal binder usage on total narcotic usage after undergoing surgery. To determine if abdominal binder usage results in decreased visual analog scale (VAS) pain scores and shorter time to first ambulation post operatively.
Interventions
- DEVICE Abdominal binder
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 36 participants |
| Start Date | 2017-10-30 |
| Est. Completion | 2021-03-22 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03684304
The ClinicalTrials.gov registry entry for NCT03684304 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 36 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University Hospitals Cleveland Medical Center, which has 230 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Abdominal binder is the first listed.
NCT03684304 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT03684304 about?
NCT03684304 is a clinical study titled "The Effect of Abdominal Binder Use on Postoperative Pain and Mobility in Patients Undergoing Pelvic Surgery". To determine the effect of post-operative abdominal binder usage on total narcotic usage after undergoing surgery. To determine if abdominal binder usage results in decreased visual analog scale (VAS) pain scores and shorter time to first ambulation post operatively.
What is the current status of trial NCT03684304?
This trial is currently terminated. It is a NA study. The enrollment target is 36 participants. The study started on 2017-10-30. Estimated completion is 2021-03-22.
What interventions are being tested in trial NCT03684304?
The interventions under investigation include: Abdominal binder (DEVICE).
Who is sponsoring clinical trial NCT03684304?
This trial is sponsored by University Hospitals Cleveland Medical Center, which has 230 total clinical trials registered on ClinicalTrials.gov.
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