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