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The purpose of this study is to determine whether propranolol can decrease pain symptoms in a common subset of patients admitted to a trauma center after injury.
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Lead Sponsor
University of North Carolina, Chapel Hill
NCT06386003 · Post Traumatic Stress Disorder, PTSD, and more
NCT07175025 · PTSD - Post Traumatic Stress Disorder, PTSD (Childbirth-Related)
NCT07082218 · Concussion (Diagnosis), Concussion, Mild Traumatic Brain Injury, and more
NCT05929911 · Post Traumatic Stress Disorder (PTSD), HIV
NCT05358067 · Post-traumatic Stress Disorder
University of North Carolina Trauma Center
Chapel Hill, North Carolina
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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