Biliary Colic Clinical Trial
Official title:
Assessment of the Analgesic Efficacy of Intravenous Ibuprofen in Biliary Colic
The aim of this study is to assess the analgesic efficacy of intravenous ibuprofen given in the Emergency Department for the treatment of biliary colic. We hypothesize that intravenous ibuprofen will provide a clinically significant drop in self-reported patient pain level as measured by the visual analog scale.
It is estimated over 20 million people aged 20-74 have gallbladder disease, with biliary
colic being a common and painful symptom in these patients. Likely due to the relatively
recent approval of intravenous ibuprofen use for fever and pain in adults, no assessment of
its analgesic efficacy for biliary colic currently exists in the literature.
Utilizing a visual analog scale (VAS) for patient self-assessment of pain, this study will
address this lack of evidence and identify intravenous ibuprofen's value as a novel analgesic
in the treatment of biliary colic. Patients will be given a VAS at the time of study therapy
administration, at 15-minute intervals during the first hour post-administration, and
30-minute intervals in the second hour. Though NSAID's have been extensively studied in the
management of this phenomenon, this study aims to help optimize pain treatment of patients
presenting to the Emergency Department with biliary colic, and potentially pave the way for
future analgesic treatment comparison studies.
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