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Effects of Propofol and Ketofol (Ketamine-Propofol mixture) on Emergence Agitation in Childre

Phase 2
Conditions
postanesthesia agitation.
Factors influencing health status and contact with health services
Registration Number
IRCT2017082829414N3
Lead Sponsor
Vice chancellor for research, Zanjan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
87
Inclusion Criteria

Inclusion criteria are: age between 3-12 years old; ASA class I and II and elective tonsillectomy. Exclusion criteria are: increased intracranial or intraocular pressure; porphyria; hepatic dysfunction; allergy to eggs or soybeans; history of psychiatric disorder; upper respiratory tract infection.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Postanesthesia agitation. Timepoint: On arrival and after 10 and 30 min stay in recovery. Method of measurement: Pediatric Anesthesia Emergence Delirium.
Secondary Outcome Measures
NameTimeMethod
aryngospasm. Timepoint: First 30 min in recovery. Method of measurement: By anesthesiologist.;Bronchospasm. Timepoint: First 30 min in recovery. Method of measurement: By anesthesiologist.;Patients requiring sedative. Timepoint: First 30 min in recovery. Method of measurement: By anesthesiologist.;Bleeding. Timepoint: First 30 min in recovery. Method of measurement: By anesthesiologist.
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