Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
Healthy Volunteers
NCT04094701

Hip Arthroscopy Postoperative Opioid Demands

Led by Rush University Medical Center · Updated on 2025-08-07

170

Participants Needed

1

Research Sites

331 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study will be a prospective, single-blinded, randomized controlled trial (RCT), investigating the influence of the number of opioid pills prescribed following primary hip arthroscopy. All patients who sign the consent form will be enrolled in the suited and randomized to one of the two treatment arms. The intervention group will receive 5 Norco pills, gabapentin (30 mg, once daily for 10 days following surgery), and Tylenol (1000 mg, three times daily for 10 days following surgery) while the control will receive the standard at our practice of 30 Norco pills.

CONDITIONS

Official Title

Hip Arthroscopy Postoperative Opioid Demands

Who Can Participate

Age: 18Years - 80Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patients age 18-80 years
  • English speaking
  • Opioid naive patient (not taking opioid pills within 6 weeks prior to surgery), confirmed by prescription monitoring
  • Undergoing primary hip arthroscopy
  • Provided written and informed consent for study participation
Not Eligible

You will not qualify if you...

  • Under 18 years of age
  • Opioid tolerant patients
  • Revision hip surgery
  • Prior infections of the operative joint
  • History of active cancer within the past 5 years
  • Chronic pain conditions including low back pain, chronic pain syndrome, fibromyalgia
  • History of alcohol or substance use disorder
  • Other diseases including rheumatologic conditions, diabetes, thyroid disorders, depression, anxiety
  • Grade IV cartilage defects

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Rush University Medical Center

Chicago, Illinois, United States, 60612

Actively Recruiting

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Research Team

C

Carla M. Edwards

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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