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Clinical Trials/NCT02904993
NCT02904993
Terminated
N/A

Prospective Randomized Study Comparing Regional Anesthetic Blocks and Periarticular Infiltration for the Management of Post-operative Pain After Direct Anterior Total Hip Replacement

Mayo Clinic1 site in 1 country9 target enrollmentMay 2016

Overview

Phase
N/A
Intervention
Not specified
Conditions
Degenerative Joint Disease
Sponsor
Mayo Clinic
Enrollment
9
Locations
1
Primary Endpoint
Changes in pain score
Status
Terminated
Last Updated
9 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
May 2016
End Date
October 2016
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

John M. Redmond, M.D.

Orthopedic Consultant

Mayo Clinic

Eligibility Criteria

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

Outcomes

Primary Outcomes

Changes in pain score

Time Frame: post-operative to 7 days

Static and dynamic post-operative pain scores, measured on a 1 - 10 visual analogue scale.

Study Sites (1)

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