ClinicalTrials.Veeva

Menu

NSAID vs. Narcotics

NYU Langone Health logo

NYU Langone Health

Status

Completed

Conditions

Multimodal Analgesia
Nonsteroidal Anti-inflammatory Drugs

Treatments

Drug: Ibuprofen 600 mg
Drug: standard oxycodone/acetaminophen

Study type

Observational

Funder types

Other

Identifiers

NCT02915055
16-01645

Details and patient eligibility

About

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.

The primary objective of the study is to compare patients' reported pain and narcotic use following meniscectomy, and determine if NSAIDs can provide adequate pain relief.

Enrollment

77 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Must be at least 18 years of age
  • ASA class I-II
  • Patients scheduled for meniscectomy

Exclusion criteria

  • Contraindication to ibuprofen or oxycodone/acetaminophen (e.g. hypersensitivity, history of GI or bleeding disorder)
  • Legally incompetent or mentally impaired (e.g. minors, Alzheimer's subjects, dementia, etc.)
  • Younger than 18 years of age or older than 65
  • Any patient considered a vulnerable subject
  • Patients on pain medication prior to surgery

Trial design

77 participants in 1 patient group

Patients with pain following knee arthroscopic meniscectomy
Treatment:
Drug: standard oxycodone/acetaminophen
Drug: Ibuprofen 600 mg

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems