Survey of effect of Dexmedetomidine on children undergoing Adenotonslectomy ;

Phase 3

Recruiting

• Conditions: Chronic tonsillitis and adenoiditis.; Chronic tonsillitis and adenoiditis; J35.0

• Registration Number: IRCT20200325046853N1
• Lead Sponsor: Esfahan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 18 May 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 105

Inclusion Criteria

3-10 year old childern candidates for adenotonsillectomy
Children who fall into the ASAI, ASAII group in terms of physical condition to determine the risk of anesthesia
Consent to participate in the study

Exclusion Criteria

Includes any underlying disease (heart-lung disease, kidney, glands, etc.)
Bleeding disorders
Impaired coagulation tests (PT, PTT, INR)
Metabolic disorders (phenylketonuria, galactasomy, etc.).

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Agitation rate. Timepoint: Every 15 minutes in recovery. Method of measurement: Paediatric Anesthesia Emergence Delirium score.;Sedation rate. Timepoint: Every 15 minutes in recovery. Method of measurement: Ramsay Sedation Scale score.;Length of stay in recovery. Timepoint: Every 15 minutes in recovery. Method of measurement: Modified Aldrete Score.;Spo2. Timepoint: Before and during anesthesia Every 15 minutes in recovery. Method of measurement: by Pulse oximetr.;Blood pressure. Timepoint: Before and during anesthesia Every 15 minutes in recovery. Method of measurement: By manometer.;Heart rate. Timepoint: Before and during anesthesia Every 15 minutes in recovery. Method of measurement: manually.;Bleeding volume. Timepoint: During surgery. Method of measurement: In milliliter.;Average dose of propofol for the treatment of delirium. Timepoint: During recovery. Method of measurement: milligram per kilogram.