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

Maternal and Child Health Hospital of Hubei Province

Status: Enrolling

Conditions: Adenotonsillectomy; Propofol; Ciprofol

Treatments: Other: Propofol group; Other: Ciprofol group

Study type: Interventional

Funder types: Other

Identifiers

NCT06882980

MCHH_008

Details and patient eligibility

About

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.

Enrollment: 236 estimated patients

Sex: All

Ages: 3 to 11 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• ASA I/II, age 3-11 years, weight 13-50 kg.

Endoscopic T&A or adenoidectomy.

Exclusion criteria

• Recent upper respiratory infection.

Difficult airway, organ dysfunction, developmental/psychiatric disorders.

Drug allergies.

Trial design

Primary purpose: Other

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Triple Blind

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236 participants in 2 patient groups

Ciprofol group

Experimental group

Description:

Ciprofol group patients will be given ciprofol during anesthesia induction and maintenance

Treatment:

Other: Ciprofol group

Propofol group

Active Comparator group

Description:

Propofol group patients will be given propofol during anesthesia induction and maintenance

Treatment:

Other: Propofol group