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Endotracheal Intubation With Sevoflurane in Surgical Pediatric Patients

NCT02429323 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2015-04-29

No results posted yet for this study

Summary

Aim of the study is to compare the optimal time needed for successful tracheal intubation with immediate 8% sevoflurane and incremental sevoflurane induction in surgical pediatric patients undergoing adenotonsillectomy without using muscle relaxants or opioids

Conditions

  • Anesthesia; Reaction

Interventions

DRUG

Sevoflurane

use of 8% sevoflurane in compared to incremental dose increased each few breaths from 1% to 8%

Sponsors & Collaborators

  • University of Sulaimani

    lead OTHER

Principal Investigators

  • Amir M. Boujan, board · School of Medicine

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
2 Years
Max Age
7 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-06-30
Primary Completion
2011-09-30
Completion
2011-11-30

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02429323 on ClinicalTrials.gov