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Study identifier: NCT06882980 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

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

Condition: Adenotonsillectomy · Propofol · Ciprofol  ·  Sponsor: Maternal and Child Health Hospital of Hubei Province

PhaseNA
Planned participants236
Who can joinAll sexes, 3 Years to 11 Years
Healthy volunteersYes

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Na Li, MD  ·  Telephone: Telephone:+86276349  ·  Email:lina@hbfy.com

Always discuss trial participation with your own doctor first.

Locations (1)

Maternal and Child Health Hospital of Hubei ProvinceWuhan, Hubei, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT06882980