Clinical Trial

Comparison of Ciprofol and Propofol Under IoC1 and IoC2 Monitoring for Adenotonsillectomy

Recruiting
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Record status
This record was last updated June 12, 2025 (before its estimated October 22, 2025 completion). Its status may not reflect the trial's current state.
Summary
The goal of this clinical trial is to compare the Ciprofol and Propofol Under IoC1 and IoC2 Monitoring for Adenotonsillectomy Participants will be randomly allocated to two groups: Ciprofol group (Group C) and Propofol group (Group P). For those in Group C: they will be given ciprofol during anesthesia induction and maintenance .For those in Group P: they will be pgiven ciprofol during anesthesia induction and maintenanc This study evaluates ciprofol versus propofol under IoC1/IoC2 guidance in pediatric T\&A, providing evidence for ciprofol's efficacy and safety in pediatric anesthesia.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2025-03-15.
Trial Details
NCT Number NCT06882980
Lead Sponsor Maternal and Child Health Hospital of Hubei Province
Conditions Adenotonsillectomy, Propofol, Ciprofol
Enrollment 236 participants
Start Date 2025-02-22
Primary Completion 2025-10-22 (estimated)
Study Completion 2025-11-22 (estimated)
Updated on ClinicalTrials.gov 2025-06-12