Geneva, March 20 -- International Clinical Trials Registry received information related to the study (ChiCTR2600119493) titled 'Comparative Observation of the Analgesic Efficacy of Anrikefon and Fentanyl in Painless Induced Abortion Surgery: A Prospective, Single-Center, Blinded, Randomized Controlled Trial' on Feb. 27.
Study Type: Interventional study
Study Design:
Parallel
Primary Sponsor: The First People's Hospital of Yunnan Province
Condition:
Painless abortion surgery pain
Intervention:
Anrikefon(A) Group:Group A received an intravenous bolus of Anruikefen at the 95% effective dose ( calculated based on body weight), followed by an intravenous bolus of propofol at 2 mg/kg.
Recruitment Status: Not Recruiting
Phase: N/A
D...