Multimodal Analgesic Regimen for Total Hip Arthroplasty: An Initiative to Minimize Postoperative Opioid Use

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorHenry Ford Health System

About this trial

This study examines whether patients undergoing total hip replacement surgery can manage their pain effectively while using fewer opioid pain medications. Participants will be randomly assigned to one of two groups. The first group will receive the standard postoperative pain medication regimen, with all prescriptions sent directly to their pharmacy as usual. The second group will receive the same medications, but their opioid prescription will only be provided as a printed copy rather than being sent directly to the pharmacy, requiring them to choose whether to fill it. All participants will keep a pain journal and complete questionnaires about their medication intake over the first 21 days post-op as well as there function and wellbeing at follow up visits over 3 months. The goal is to determine whether this approach reduces opioid use while still adequately controlling pain after hip replacement surgery.

Eligibility criteria

Qualifiers

Adult patients age 18 and older

Patients who have undergone total hip arthroplasty by a single, fellowship trained Orthopaedic Surgeon.

Disqualifiers

Patients with incomplete data in medical records

Chronic opioid use in the last 3 months

Ipsilateral joint surgery in the last year

Cannot tolerate oral medications

Trial design

Treatments tested in this trial

  • Standard Multimodal Analgesic Regimen with Opioid Prescription
  • Opioid-Reduced Multimodal Analgesic Regimen with Printed Prescription

Treatment groups

100 Participants
are divided into 2 treatment groups

Sponsors and collaborators