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NCT03825809 · ClinicalTrials.gov registry record · Phase 2
Nonopioid Analgesia After Labral Surgery
A Phase 2 study of Narcotic Use, sponsored by Henry Ford Health System.
- Recruiting
- Registry status
- Phase 2
- Development phase
- 100
- Enrollment target
- 1
- Study location
NCT03825809: Recruiting Phase 2 study of Narcotic Use, sponsored by Henry Ford Health System.
NCT03825809 is a Phase 2 study of Narcotic Use that is actively recruiting participants, run by Henry Ford Health System. The registered enrollment target is 100 participants, roughly in line with the 101-participant average among 3 other Narcotic Use trials with a reported enrollment target. The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT03825809, a Phase 2 study of Narcotic Use, is actively recruiting participants, sponsored by Henry Ford Health System.
- RECRUITING
- Registry status
- Phase 2
- Development phase
- 100 participants
- Enrollment target
- 1
- Study location
Study Summary
This is a randomized, single blinded, standard of care controlled clinical trial. This project aims to compare postoperative pain control in patients in two treatment arms of rotator cuff repair: a treatment group given a nonopioid pain control regimen, and a standard of care control group given standard opioid pain control regimen
Primary Outcome
Patients recorded pain levels 3 times per day using Visual analog scales until study completion. Average daily pain was calculated for each patient. Higher values portend worse control.
Conditions Studied
Interventions
- DRUG Acetaminophen
- DRUG Ketorolac
- DRUG Celecoxib
- DRUG Gabapentin
- DRUG Hydrocodone-Acetaminophen
Study Locations (1)
Michigan
- Henry Ford Health System - Detroit
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2019-01-22 |
| Est. Completion | 2020-05-20 |
| Phase | Phase 2 |
What NCT03825809 shows while recruiting
NCT03825809 is an interventional study that assigns participants to a tested intervention. The registered 100 participants enrollment target is mid-sized for trials with a published cap, roughly in line with the 101-participant average among 3 other Narcotic Use trials with a reported enrollment target.
The record links to 1 condition, with Narcotic Use appearing as the primary indexed condition, and to 5 interventions - of which Acetaminophen is the first listed.
NCT03825809 reports a single indexed study location in Michigan.
Frequently Asked Questions
What is clinical trial NCT03825809 about?
NCT03825809 is a clinical study titled "Nonopioid Analgesia After Labral Surgery". This is a randomized, single blinded, standard of care controlled clinical trial. This project aims to compare postoperative pain control in patients in two treatment arms of rotator cuff repair: a treatment group given a nonopioid pain control regimen, and a standard of care control group given sta...
What is the current status of trial NCT03825809?
This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 100 participants. The study started on 2019-01-22. Estimated completion is 2020-05-20.
What conditions does trial NCT03825809 study?
This clinical trial studies the following conditions: Narcotic Use.
What interventions are being tested in trial NCT03825809?
The interventions under investigation include: Acetaminophen (DRUG), Ketorolac (DRUG), Celecoxib (DRUG), Gabapentin (DRUG), Hydrocodone-Acetaminophen (DRUG).
Who is sponsoring clinical trial NCT03825809?
This trial is sponsored by Henry Ford Health System, which has 234 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03825809 being conducted?
This trial has 1 study location across Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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