Overview

Study to Test the Efficacy of Periarticular Levo Bupivicaine Injection Following Primary Hip Arthroplasty

Status:
Completed
Trial end date:
2009-09-01
Target enrollment:
0
Participant gender:
All
Summary
The hypothesis of this study is that isolated use of local periarticular levobupivicaine injection during primary hip arthroplasty would improve post-operative pain control. Patients were randomised in the operating room to receive either a periarticular infiltration, or a placebo consisting of Saline. Morphine and analgesic consumption was recorded for each patient, while the modified McGill pain scale was used to determine the adequacy of analgesia and the benefit of the peri-articular infiltration. 91 patients were recruited, with 45 patients in the treatment group and 46 controls. The results were assessed after one year, once all the information from both treatment groups was collected.
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Orthopaedic Research and Innovation Foundation
Orthopaedic Research and Innovation Foundation, Ireland
Treatments:
Bupivacaine
Levobupivacaine
Criteria
Inclusion Criteria:

- Consecutive patients undergoing primary hip arthroplasty for osteoarthritis only were
included in this study after giving informed consent.

Exclusion Criteria:

- Patients with cognitive impairment, neurological disorders, advanced liver or renal
impairment, known ischemic heart disease, a previous diagnosis of a pain syndrome or
any post-operative surgical or medical complications were excluded.