Pain Relief After Trapeziectomy: Ibuprofen & Acetaminophen Versus Oxycodone
- Conditions
- Pain, PostoperativeOsteoarthritis Thumb
- Interventions
- Drug: NSAID capsulesDrug: Opioid capsule
- Registration Number
- NCT04676802
- Lead Sponsor
- Stanford University
- Brief Summary
In the US, pain management after surgery for surgical treatment of osteoarthritis at the base of the thumb typically consists of prescription opioids during the early recovery phase. Given the highly addictive nature of prescription opioids, guidelines are being evaluated by hand surgeons to reduce opioid use while still maintaining pain control after surgery. A promising approach is to use non-narcotic medication as the first line of treatment. The purpose of this study is to demonstrate the efficacy of a combination of non-steroidal anti-inflammatory drugs (NSAIDs), ibuprofen and acetaminophen, in comparison to a morphine analogue substance (oxycodone) for pain management in the first 30 days after surgery.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 121
- Undergoing trapeziectomy for thumb osteoarthritis
English proficient,
- Pregnancy
Current use of opioids
Concurrent surgeries (ex. trapeziectomy combined with carpal tunnel release)
Inability to complete study forms (education, cognitive ability, mental status, medical status)
Allergy or intolerance to Ibuprofen, Acetaminophen and/or Oxycodone
Liver or kidney dysfunction, abnormal liver enzymes restricting use of acetaminophen or ibuprofen
History of chronic heart failure, upper gastrointestinal bleeding or coagulopathy
History of complex regional pain syndrome
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description NSAIDS NSAID capsules Following surgery will receive NSAID capsules following surgery. Will take online and phone surveys. Opioids Opioid capsule Following surgery will receive opioid capsules following surgery. Will take online and phone surveys.
- Primary Outcome Measures
Name Time Method Change of medication consumption and overall amount Every day from the first day after surgery to 30 days post-op. The number of capsules consumed in the last 24 hours. Consumption rate and overall consumption will be compared between groups to assess efficacy and inform further statistical analyses.
Change of worst daily pain score measured over time Every day from the first day after surgery to 30 days post-op. Numerical score describing surgical pain at its worst in the last 24 hours, between 1 and 10, 1 being no pain, 10 being the worst possible pain.
Change of least daily pain score measured over time Every day from the first day after surgery to 30 days post-op. Numerical score describing surgical pain at its least in the last 24 hours, between 1 and 10, 1 being no pain, 10 being the worst possible pain.
Change of average daily pain score measured over time Every day from the first day after surgery to 30 days post-op. Numerical score describing average surgical pain in the last 24 hours, between 1 and 10, 1 being no pain, 10 being the worst possible pain.
- Secondary Outcome Measures
Name Time Method Change in Quick DASH scores over time Baseline, Post-operative weeks 1, 3, 5, and 8 Quick Disabilities of the Arm, Shoulder, and Hand (qDASH) is a responsive measure to patient-reported functional change in the hand and upper extremity patient population, ranging from 0 to 100. Lower scores signify limited function and increased pain.
Change in PROMIS-PI scores over time Baseline, Post-operative weeks 1, 3, 5, and 8 PROMIS-PI scores (Patient-Reported Outcomes Measurement Information System - Pain Interference) are effective measures of the change in perceived pain, supporting intervention related studies assessing power analyses for comparative research.
We use the Pain Interference - Short Form version 6b, which consists of 6 questions regarding how much the pain experienced in the last 7 days interfered with everyday aspects of life (i.e. enjoyment, ability to concentrate, day to day activities, recreational activities, doing tasks away from home, and socializing with others). The answers to all questions are ordinals ranging from 1 (not interfered at all) to 5 (interfered very much).
Trial Locations
- Locations (2)
Stanford Health Care
🇺🇸Redwood City, California, United States
University of Utah Health Care
🇺🇸Salt Lake City, Utah, United States