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NCT04018768 · ClinicalTrials.gov registry record
Multimodal Analgesia With NSAID vs. Narcotics Alone After Shoulder Instability Surgery
A clinical trial, sponsored by NYU Langone Health.
- Completed
- Registry status
- 80
- Enrollment target
NCT04018768 is a clinical trial that has completed, run by NYU Langone Health. The registered enrollment target is 80 participants.
The verdict
NCT04018768 has completed, sponsored by NYU Langone Health.
- COMPLETED
- Registry status
- 80 participants
- Enrollment target
Study Summary
This will be a single-center, prospective observational study. The study will compare post- operative pain scores and narcotic consumption between two groups of patients - one cohort will receive ibuprofen (Motrin) and Percocet (to be used as needed) while the other cohort will receive only Percocet. Both pain management options are considered to be standard of care.
Interventions
- OTHER ibuprofen 600 mg
- OTHER Oxycodone/acetaminophen (Percocet) 5 mg/325
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 80 participants |
| Start Date | 2017-12-01 |
| Est. Completion | 2019-02-01 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04018768
The ClinicalTrials.gov registry entry for NCT04018768 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 80 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is NYU Langone Health, which has 1,164 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which ibuprofen 600 mg is the first listed.
NCT04018768 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT04018768 about?
NCT04018768 is a clinical study titled "Multimodal Analgesia With NSAID vs. Narcotics Alone After Shoulder Instability Surgery". This will be a single-center, prospective observational study. The study will compare post- operative pain scores and narcotic consumption between two groups of patients - one cohort will receive ibuprofen (Motrin) and Percocet (to be used as needed) while the other cohort will receive only Percocet...
What is the current status of trial NCT04018768?
This trial is currently completed. The enrollment target is 80 participants. The study started on 2017-12-01. Estimated completion is 2019-02-01.
What interventions are being tested in trial NCT04018768?
The interventions under investigation include: ibuprofen 600 mg (OTHER), Oxycodone/acetaminophen (Percocet) 5 mg/325 (OTHER).
Who is sponsoring clinical trial NCT04018768?
This trial is sponsored by NYU Langone Health, which has 1,164 total clinical trials registered on ClinicalTrials.gov.
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