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RECRUITING
NCT06882980
NA

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

Sponsor: Maternal and Child Health Hospital of Hubei Province

View on ClinicalTrials.gov

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.

Key Details

Gender

All

Age Range

3 Years - 11 Years

Study Type

INTERVENTIONAL

Enrollment

236

Start Date

2025-02-22

Completion Date

2025-11-22

Last Updated

2025-06-12

Healthy Volunteers

Yes

Interventions

OTHER

Ciprofol group

In the Ciprofol group,children were given Ciprofol 0.6-0.8 mg/kg during anesthesia induction,and ciprofol 1.2-2 mg·kg-¹·h-¹for anesthesia maintenance.Throughout the entire process, we continuously monitor vital signs and IoC1/IoC2.

OTHER

Propofol group

In the Propofol group,children were given Propofol 2.5-3.5 mg/kg during anesthesia induction,and propofol 6-10 mg·kg-¹·h-¹for anesthesia maintenance.Throughout the entire process, we continuously monitor vital signs and IoC1/IoC2.

Locations (1)

Maternal and Child Health Hospital of Hubei Province

Wuhan, Hubei, China