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Comparison of the effect of dexmedetomidine and atracurium in the ease of the tracheal after induction with propofol and sufentanil in children aged 6 to 12 years without neuromuscular relaxants

Phase 3
Conditions
Comparison of the effect of dexmedetomidine and atracurium in the ease of the tracheal after induction with propofol and sufentanil in children aged 6 to 12 years without neuromuscular relaxants.
Failed or difficult intubation
T88.4
Registration Number
IRCT20201028049177N1
Lead Sponsor
Mashhad University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
50
Inclusion Criteria

Age between six to twelve years
Candidates for tracheal intubation under general anesthesia who are candidates for elective surgery
Asa physical condition score one and two
Consent of the patient's guardian or legal guardian to enter the study

Exclusion Criteria

Respiratory tract infection three weeks before intubation
Children with cardiovascular disease
Children have a difficult airway for intubation
Children with morbid obesity (weight to height ratio more than 20%)
Children with neuromuscular diseases
Dissatisfaction of parents or legal guardians of patients to enter the study

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Success rate in intubation. Timepoint: before intervention and 1 min after intervention. Method of measurement: Ease of intubation based on scoring table and intubation anesthesia partner checklist. Vital signs were recorded by monitoring. Includes sphygmomanometer .Pulse oximetry .Electrocardiogram.;Success rate in intubation in two groups/Hemodynamic responses. Timepoint: At zero time: before induction time one after induction and before intubation and time two one minute after intubation. Method of measurement: Scoring table / monitoring of blood pressure, heart rate and pulse oximetry.
Secondary Outcome Measures
NameTimeMethod
Secondary outcomes include hemodynamic responses at time zero: before induction, time one after induction and before intubation, and two minutes one minute after intubation measured in both groups and the incidence of complications in both groups and scoring the intubation status (scoring). Timepoint: before intervention and 1 min after intervention. Method of measurement: the scoring method.
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