Pain Management After Shoulder Prosthesis: A Clinical Trial of Nerve Block and Local Infiltration
Not Applicable
Terminated
- Conditions
- Pain, Postoperative
- Interventions
- Procedure: Interscalene catheterProcedure: Local infiltration analgesia
- Registration Number
- NCT01362075
- Lead Sponsor
- Horsens Hospital
- Brief Summary
The purpose of this study is to determine the efficacy of local infiltration analgesia as compared to 48-hour interscalene block in treating pain after shoulder arthroplasty. The investigators hypothesize a reduced pain score and use of supplemental analgesic medication during the first three postoperative days using local infiltration analgesia.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- All
- Target Recruitment
- 74
Inclusion Criteria
- elective primary shoulder arthroplasty
Exclusion Criteria
- reverse or delta prosthesis
- recent fracture near the shoulder
- allergic to amid-type local analgesics
- operation not under general anaesthesia
- incompetent, pregnant, below 18 or above 90 years old
- severe chronic neurogenic pain or sensory disturbances in the shoulder
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Interscalene catheter Interscalene catheter - Local infiltration analgesia Local infiltration analgesia -
- Primary Outcome Measures
Name Time Method Supplemental analgesics ingested First 24 hours postoperatively
- Secondary Outcome Measures
Name Time Method Pain score First 72 hours postoperatively Supplemental analgesics ingested First 72 hours postoperatively
Trial Locations
- Locations (2)
Aarhus University Hospital, Aarhus Hospital
🇩🇰Aarhus, Denmark
Horsens Hospital
🇩🇰Horsens, Denmark