Interventional
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
pain score during cough
pain score during cough at 24 hours after TAP block (using visual analog scale)
24hr after TAP block
Yes
Korea: Institutional Review Board
NCCCTS-11-557
NCT01423292
August 2011
April 2012
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