Clavicle Fracture Clinical Trial
Official title:
Does Liposomal Bupivacaine Provide Improved Pain Management for ORIF of Midshaft Clavicle Fractures?
Verified date | October 2018 |
Source | University of Minnesota - Clinical and Translational Science Institute |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
To determine whether liposomal bupivacaine wound infiltration decreases pain scores and narcotic use when compared to bupivacaine alone after open reduction internal fixation of midshaft clavicle fractures.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | January 1, 2018 |
Est. primary completion date | January 1, 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Mid-shaft Clavicle Fracture treated with ORIF Exclusion Criteria: - Unable to be contacted for 72 hours post surgery - Other concurrent surgical procedures - Chronic narcotic user |
Country | Name | City | State |
---|---|---|---|
United States | University of Minnesota | Minneapolis | Minnesota |
Lead Sponsor | Collaborator |
---|---|
University of Minnesota - Clinical and Translational Science Institute |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Visual Analogue Pain Scale Averages between the two treatments | Scale is based on 1-10 with 1 being the lowest pain and 10 being the highest pain. | 72 hours post surgery |
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