Local Infiltration Analgesia With Ropivacaine Versus Placebo in Bilateral Hip Arthroplasty
Phase 4
- Conditions
 - Hip ArthroplastyPostoperative Pain
 
- Interventions
 - Drug: saline.9%
 
- Registration Number
 - NCT00864409
 
- Lead Sponsor
 - Hvidovre University Hospital
 
- Brief Summary
 High-volume infiltration analgesia may be effective in postoperative pain management following total hip arthroplasty. In this randomized, double-blind trial patients undergoing bilateral hip arthoplasty are randomized to receive high-volume local anesthetic infiltration in one hip and similar infiltration with saline (placebo) in the other hip.
- Detailed Description
 Not available
Recruitment & Eligibility
- Status
 - UNKNOWN
 
- Sex
 - All
 
- Target Recruitment
 - 12
 
Inclusion Criteria
- scheduled for bilateral total hip arthroplasty
 - able to speak and understand Danish
 
Exclusion Criteria
- treatment with opioids or steroids
 
Study & Design
- Study Type
 - INTERVENTIONAL
 
- Study Design
 - Not specified
 
- Arm && Interventions
 Group Intervention Description Hip 1 ropivacaine 0,2% high volume local anesthetic infiltration Hip 2 saline.9% - 
- Primary Outcome Measures
 Name Time Method postoperative pain 0-48 hours postoperative 
- Secondary Outcome Measures
 Name Time Method 
Trial Locations
- Locations (1)
 Hviovre University Hospital
🇩🇰Hvidovre, Denmark
Hviovre University Hospital🇩🇰Hvidovre, DenmarkLasse Andersen, MDContact+45 36323632lasse.oestergaard.andersen@hvh.regionh.dk
