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

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

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600124122
Enrollment
Unknown
Registered
2026-05-07
Start date
2025-02-24
Completion date
Unknown
Last updated
2026-05-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adenotonsillectomy

Interventions

ciprofol group:Intraoperative induction and maintenance with ciprofol
propofol group:Intraoperative induction and maintenance with propofol

Sponsors

Maternal and Child Health Hospital of Hubei Province
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 11 Years

Inclusion criteria

Inclusion criteria: 1. ASA class I or II 2. Age 3 to 11 years (including 3 and 11 years) 3. Weight 13 to 50 kg (including 13 kg and 50 kg) 4. Planned Adenotonsillectomy.

Exclusion criteria

Exclusion criteria: 1. Recent upper respiratory tract infection; 2. Preoperative assessment of difficult airway; 3. Combined cardiac, pulmonary, brain, liver, kidney and other vital organ dysfunction; 4. Developmental delay, mental abnormalities that cannot match the scale score; 5. Allergies to drugs used in this research institute.

Design outcomes

Primary

MeasureTime frame
sedation/consciousness (IoC1),analgesia/pain-stress (IoC2);The time to loss of consciousness during anesthesia induction;Induction Compliance checklist(ICC);

Secondary

MeasureTime frame
Mean arterial pressure;Heart rate;Pediatric Anesthesia Emergence Delirium (PAED) Scale;Adverse events;anesthetist satisfaction;record real-time values;

Countries

China

Contacts

Public ContactHongbo Deng

Maternal and Child Health Hospital of Hubei Province

1587188130@qq.com+86 158 2733 8895

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 16, 2026