RecruitingNot ApplicableNCT04094701

Hip Arthroscopy Postoperative Opioid Demands

Randomized Control Trial Evaluating Postoperative Opioid Demands Following Hip Arthroscopy


Sponsor

Rush University Medical Center

Enrollment

170 participants

Start Date

Oct 21, 2020

Study Type

INTERVENTIONAL

Conditions

Summary

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.


Eligibility

Min Age: 18 YearsMax Age: 80 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying Control Group Regimen and Opioid reduced regimen for people with femoral acetabular impingement, labral tear, glenoid, and other related conditions. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years to 80 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

OTHERControl Group Regimen

Norco (hydrocodone-acetaminophen) 5mg-325mg, 30 total pills. This is the standard of care prescribing procedure for pain management after hip arthroscopy.

OTHEROpioid reduced regimen

Tylenol extra strength (1000 mg, three times daily for 10 days following surgery), Gabapentin (300 mg at night for 10 days following surgery) and Norco (hydrocodone-acetaminophen) 5mg-325mg, 5 total pills


Locations(1)

Rush University Medical Center

Chicago, Illinois, United States

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NCT04094701


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