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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: Completed study, sponsored by NYU Langone Health.
NCT04018768 is a clinical trial that has completed, run by NYU Langone Health. The registered enrollment target is 80 participants. According to ClinicalTrials.gov, the official US trial registry.
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.
Primary Outcome
Scale consisting of a drawn line from 0 to 100 - the patient will be asked to mark where they believe their pain is (100 being worse pain).
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 |
What the finished NCT04018768 record still lists
NCT04018768 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 80 participants, a relatively small participant target.
The record links to 0 conditions, and to 2 interventions - of which ibuprofen 600 mg is the first listed.
NCT04018768 does not publish any study locations in the registry export this page uses.
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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