Effect of two drugs, propofol and fentanyl in controlling emergence agitation following anesthesia with sevoflurane gas

Phase 3

Recruiting

• Conditions: Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified; agitation due to sevoflurane gas.

• Registration Number: IRCT20181130041804N1
• Lead Sponsor: Sanandaj University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 25 February 2019

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

Children aged 2 to 10 years old
Class one or two of ASA
Children under general anesthesia with sevoflurane

Exclusion Criteria

Children with growth retardation
Children with psychological diseases
Children with neurological disease
Children with abnormal airway
Irritable children

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Agitation Score. Timepoint: 5 ,10 ,15 ,20 minute after the treatment of Agitation. Method of measurement: RASS (Richmond agitation sedation scale).

Secondary Outcome Measures

Name	Time	Method
Vomiting. Timepoint: 5,10,15,20 minutes after injection of propofol or fentanyl. Method of measurement: In the form of positive or Negative by watching and reporting the caregiver.;Nausea. Timepoint: 5,10,15,20 minutes after injection of propofol or fentanyl. Method of measurement: In the form of positive or Negative by watching and reporting the caregiver.