Comparison of Ciprofol and Propofol Under IoC1 and IoC2 Monitoring for Adenotonsillectomy
Recruiting
N/A
Interventional Study
Adenotonsillectomy
Propofol
Ciprofol
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 3 – 11
- Sex
- Any
- Study type
- Interventional
- Purpose
- Other
- Participants needed
- 236 (estimated)
- Sponsor
- Maternal and Child Health Hospital of Hubei Province · Other
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About This Trial
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 …
Trial Locations
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Eligibility Criteria
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.
Contacts