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Clinical Trial Summary

Patients between the ages of 12 months and 11 years who are undergoing an open lower abdominal procedure will be randomized to receive intrathecal morphine, or bilateral quadratus lumborum block. The investigators will compare the effect that intrathecal morphine and quadratus lumborum blocks have on the duration of pain control as demonstrated by charted pain scores and morphine equivalents in the first 48 hours. This study will also assess the side effects of each intervention such as nausea and vomiting, and itching.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05506930
Study type Interventional
Source Medical University of South Carolina
Contact Haley Nitchie, MHA
Phone 843-792-1869
Email nitchie@musc.edu
Status Recruiting
Phase Phase 4
Start date August 17, 2022
Completion date February 1, 2027

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