Nonopioid Pain Control Regimen After Arthroscopic Hip Procedures
Phase 4
Recruiting
- Conditions
- Hip Arthroscopy
- Interventions
- Registration Number
- NCT05076110
- Lead Sponsor
- Mayo Clinic
- Brief Summary
This study is being conducted to evaluate the effectiveness of post-operative pain control without using narcotic pain medications.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 188
Inclusion Criteria
• Scheduled for a primary Hip Arthroscopy at Mayo Clinic (Rochester, MN)
Exclusion Criteria
- medical history of known allergies or intolerance to allergies or intolerance to Motrin, Gabapentin, Tylenol, dexamethasone, tramadol, or Robaxin.
- Substantial alcohol or drug abuse.
- History of narcotics within 6 months of surgery.
- Pregnancy.
- Renal impairment.
- Peptic ulcer disease.
- GI bleeding.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Non-Opiate Pain Control Group Ibuprofen Subjects will receive a non-opiate pain control regime using Ibuprofen, Gabapentin, Acetaminophen, Methocarbamol for pain control following hip arthroscopy procedure. Standard of Care Group Oxycodone Subjects will receive standard of care pain medication Oxycodone for pain control following hip arthroscopy procedure Non-Opiate Pain Control Group Acetaminophen Subjects will receive a non-opiate pain control regime using Ibuprofen, Gabapentin, Acetaminophen, Methocarbamol for pain control following hip arthroscopy procedure. Non-Opiate Pain Control Group Gabapentin Subjects will receive a non-opiate pain control regime using Ibuprofen, Gabapentin, Acetaminophen, Methocarbamol for pain control following hip arthroscopy procedure. Non-Opiate Pain Control Group Methocarbamol Subjects will receive a non-opiate pain control regime using Ibuprofen, Gabapentin, Acetaminophen, Methocarbamol for pain control following hip arthroscopy procedure.
- Primary Outcome Measures
Name Time Method Change in pain score Baseline, 14 days post-operatively Measure using a visual analog scale (VAS) to rate pain on a scale 0-10; 0=no pain to 10=worst possible pain
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Mayo clinic
🇺🇸Rochester, Minnesota, United States