Pain, Postoperative Clinical Trial
Official title:
Pain Management After Shoulder Arthroplasty: A Randomised Clinical Trial of Interscalene Block and Local Infiltration Analgesia
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.
Status | Terminated |
Enrollment | 74 |
Est. completion date | October 2014 |
Est. primary completion date | July 2014 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years to 90 Years |
Eligibility |
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 |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Denmark | Aarhus University Hospital, Aarhus Hospital | Aarhus | |
Denmark | Horsens Hospital | Horsens |
Lead Sponsor | Collaborator |
---|---|
Horsens Hospital | Aarhus University Hospital, Central Denmark Region, The Danish Rheumatism Association, The Family Hede Nielsens Fund, University of Aarhus |
Denmark,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Supplemental analgesics ingested | First 24 hours postoperatively | No | |
Secondary | Pain score | First 72 hours postoperatively | No | |
Secondary | Supplemental analgesics ingested | First 72 hours postoperatively | No |
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