Study Comparing Regional Anesthetic Blocks and Periarticular Infiltration for the Management of Post-operative Pain After Direct Anterior Total Hip Arthroplasty
Not Applicable
Terminated
- Conditions
- Degenerative Joint Disease
- Registration Number
- NCT02904993
- Lead Sponsor
- Mayo Clinic
- Brief Summary
To compare two methods of post-operative pain management in patients undergoing total hip arthroplasty. There is a perception that the periarticular injections may not be as effective in controlling post-operative pain.
Both methods are current standard of care. The investigators want to compare the outcomes of each when patients are randomized to one of the methods compared to the other method of post-operative pain control.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- All
- Target Recruitment
- 9
Inclusion Criteria
- Subject scheduled for Direct Anterior unilateral total hip replacement
- Weight ≥ 50 and ≤125 kg
- Intact neurological exam
- Cognitively intact with ability to sign consent
Exclusion Criteria
- Renal insufficiency with creatinine > 1.5 mg/dl
- Allergic to any of the following : Ropivacaine, Epinephrine, Ketorolac, Morphine sulfate, NSAIDs, Tylenol, Neurontin, Morphine, Oxycodone or Dilaudid.
- Subject taking regular narcotic medications prior to surgery (20mg/day Morphine equivalents for >7days)
- Subject with prior open hip surgery who received regional anesthesia or periarticular injection for post op pain management.
- Subject with contraindication for spinal anesthesia
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Changes in pain score post-operative to 7 days Static and dynamic post-operative pain scores, measured on a 1 - 10 visual analogue scale.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Mayo Clinic in Florida
🇺🇸Jacksonville, Florida, United States
Mayo Clinic in Florida🇺🇸Jacksonville, Florida, United States