Condition: Acute Pain · Sponsor: Duke University
Evaluate the content validity and comprehensibility of a caregiver observer-reported outcome assessment and clinician-reported assessments for acute pain in children aged 0 to \<2 years. The primary objective of the Qualitative Protocol in the UH3 phase study is to establish or create reliable Clinical Outcome Assessments (COAs) and endpoints that can assess acute pain during clinical trials of pain therapeutics specifically designed for infants and young children (0 - \<2 years).
This description comes directly from the study's public registry record.
Sophie Wang, MBBS, MHS · 919-668-5971 · sophie.wang@duke.edu
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| Duke Clinical Research Institute | Durham, North Carolina, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06164028