Geneva, May 18 -- International Clinical Trials Registry received information related to the study (ChiCTR2600124188) titled 'Study on the safety and efficacy of esketamine-cipepofol-remifentanil anesthesia in non-endotracheal intubation ERCP surgery' on May 8.
Study Type: Interventional study
Study Design:
Parallel
Primary Sponsor: Huai'an First People's Hospital
Condition:
Common bile duct stones
Intervention:
Control Group:The same volume of normal saline + Propofol at 3 mg/kg/h + Remifentanil at 1.8 µg/kg/h.
Group one:Esketamine 0.1mg/kg/h + Propofol 3mg/kg/h + Remifentanil 1.8µg/kg/h
Group Two:Equal volume of normal saline + Cipepofol 0.8 mg/kg/h + Remifentanil 1.8 µg/kg/h
Recruitment Status: Not Recruiting
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