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Nonopioid Analgesia After Arthroscopic Meniscus Surgery

NCT03820193 · Status: COMPLETED · Phase: EARLY_PHASE1 · Type: INTERVENTIONAL · Enrollment: 61

Last updated 2023-12-05

No results posted yet for this 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 arthroscopic meniscus surgery: a treatment group given a non-opioid pain control regimen, and a standard of care control group given standard opioid pain control regimen

Conditions

  • Meniscus Disorder
  • Narcotic Use

Interventions

DRUG

Celecoxib

Post-Operative Non Opioid Pain Protocol

DRUG

Hydrocodon/Acetaminophen

Traditionally used narcotic pain control

DRUG

Ketorolac

Post-Operative Non Opioid Pain Protocol

DRUG

Gabapentin

Post-Operative Non Opioid Pain Protocol

DRUG

Acetaminophen

Post-Operative Non Opioid Pain Protocol

DRUG

Diazepam

Post-Operative Non Opioid Pain Protocol

Sponsors & Collaborators

  • Henry Ford Health System

    lead OTHER

Principal Investigators

  • Toufic R Jildeh, MD · Henry Ford Health System

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-01-22
Primary Completion
2020-06-20
Completion
2021-01-20
FDA Drug
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Drugs

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03820193 on ClinicalTrials.gov