ACTRN12617001546347
Completed
Phase 4
A comparison of efficacy of three techniques for regional anaesthesia in patients undergoing shoulder arthroscopy.
Orthopaedic Research Institute of Queensland0 sites130 target enrollmentNovember 9, 2017
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Orthopaedic Research Institute of Queensland
- Enrollment
- 130
- Status
- Completed
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Patients scheduled to undergo shoulder arthroscopy under the care of the investigating surgeons.
- •Male and female
- •Able to provide informed consent
- •Patients with BMI \<40
- •Patients not currently taking regular opioid analgesics
Exclusion Criteria
- •Patients with distorted anatomy that may negatively impact on block insertion
- •Patients with pre\-existing nerve injury/neuropathy affecting the innervation of the upper limb \& shoulder.
- •Patients with a known adverse drug reaction to the medications used in this study
- •Patients with comorbid medical conditions that would contraindicate block insertion (i.e. ISB in severe COPD)
- •Patients unable to comply with assessment requirements
- •Patients with active infection
- •Patients with BMI \>40
- •Patients who are pregnant or planning on becoming pregnant during the course of the study
- •Patients unable to provide informed consent
Outcomes
Primary Outcomes
Not specified
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