Pain Clinical Trial
Official title:
Comparison of Pain Relief After Single Shot Interscalene Block With Continuous Interscalene Block for Arthroscopic Rotator Cuff Shoulder Surgery: A Randomized Study
Verified date | May 2014 |
Source | University of Chicago |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Institutional Review Board |
Study type | Observational |
1. Rotator cuff have painful post surgery recovery.
2. Single shot interscalene with oral analgesics may or may not be enough
3. Continuous nerve block may be too much for the surgery
4. The idea is to compare two techniques to see if the two techniques can improve patient
pain control and satisfaction.
Status | Completed |
Enrollment | 88 |
Est. completion date | October 2013 |
Est. primary completion date | October 2013 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years to 90 Years |
Eligibility |
Inclusion Criteria: - adult - rotator cuff surgery - agreeing to regional block for pain control Exclusion Criteria: - pregnancy - neuropathy - any allergies to local anesthetics - any contraindication to nerve blocks |
Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
United States | University of Chicago Hospitals | Chicago | Illinois |
Lead Sponsor | Collaborator |
---|---|
University of Chicago |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | pain relief | Patients having rotator cuff repair surgery will be randomized to either single shot or continuous catheter group. Pain score will be followed for 2 days to see which group gets better pain relief. | 2-3 days | No |
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