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Comparison of the effect of midazolam-ketamine with ketamine-propofol on post-tonsillectomy agitation in childre

Phase 2
Conditions
Tonsillectomy.
Chronic tonsillitis
J35.01
Registration Number
IRCT20141009019470N92
Lead Sponsor
Shiraz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
150
Inclusion Criteria

ASA I-II
Airway class I-II
Normal BMI
children aged 5-15
children candidate for elective adenotonsillectomy
Isoflurane based anesthesia

Exclusion Criteria

History of neuropsychiatric illness
CHD
URTI
Seizure
Drug reactions
Any history of post operation complications
Any complication of surgery or anesthesia that could cause agitation itself

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Sedation. Timepoint: At arrival to recovery room 5 minute, 10 minute, 20 minute and on recovery room discharge. Method of measurement: Richmond Agitation & Sedation Scale (RASS).;Pain. Timepoint: At arrival to recovery room 5 minute, 10 minute, 20 minute and on recovery room discharge. Method of measurement: Objective Pain Scale (OPS).;Recover duration. Timepoint: At arrival to recovery room 5 minute, 10 minute, 20 minute and on recovery room discharge. Method of measurement: Modified Aldrete score.
Secondary Outcome Measures
NameTimeMethod
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