Geneva, March 20 -- International Clinical Trials Registry received information related to the study (CTRI/2026/02/104713) titled 'Comparison of sleep-induction time between standard and diluted Propofol for patients undergoing tubal ligation surgery' on Feb. 25.
Study Type: Interventional
Study Design:
Randomized, Parallel Group, Active Controlled Trial Method of generating randomization sequence:Computer generated randomization Method of allocation concealment:On-site computer system Blinding and masking:Participant and Investigator Blinded
Primary Sponsor: DrBabasaheb ambedkar medical college and hospital
Condition:
Health Condition 1: O- Medical and Surgical
Intervention:
Intervention1: 0.5% Propofol: 1 ml 1% Propofol dilu...