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Ketofol Efficiency against Emergency Agitation in Children Undergoing Adenotonsillectomy

Ketofol Efficiency against Emergency Agitation in Children Undergoing Adenotonsillectomy

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900023634
Enrollment
Unknown
Registered
2019-06-04
Start date
2019-07-25
Completion date
Unknown
Last updated
2019-06-11

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

Conditions

children postoperative agitation

Interventions

Experimental group:Ten minutes before the end of the operation, intravenously inject 3 ml of ketofol
Control group:Ten minutes before the end of the operation, intravenously inject 3 ml of physiological saline.

Sponsors

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
11 Years to 15 Years

Inclusion criteria

Inclusion criteria: 11-15 years of age; ASA I or II; informed consent from their guardian; planned tonsillectomy; planned to receive general anesthesia.

Exclusion criteria

Exclusion criteria: Refusal to participate in the study; clinically significant cardiovascular, respiratory, or epilepsy; operation time of more than 1 hour; allergy to the study drug or contraindications; With systemic disease, liver, kidney disease or bleeding.

Design outcomes

Primary

MeasureTime frame
the incidence rate of postoperative agitation;

Countries

China

Contacts

Public ContactYao Shanglong

Department of Anesthesiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

ysltian@163.com+86 13886128437

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026