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.
Drug: Liposomal Bupivacaine
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Full eligibility criteria for NCT03020563
Ages eligible for Study
18 Years and older
Genders eligible for Study
Accepts Healthy Volunteers
Mid-shaft Clavicle Fracture treated with ORIF
Unable to be contacted for 72 hours post surgery
Other concurrent surgical procedures
Chronic narcotic user
All locations for NCT03020563
United States (1)
University of Minnesota
Minneapolis, Minnesota, United States, 55454
View full eligibility
Tris trial is registered with FDA with number: NCT03020563. The sponsor of the trial is University of Minnesota and it is looking for 0 volunteers for the current phase.
Official trial title: Does Liposomal Bupivacaine Provide Improved Pain Management for ORIF of Midshaft Clavicle Fractures?
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