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Clinical Trials/IRCT20171030037093N20
IRCT20171030037093N20
Recruiting
Phase 2

Evaluation of the Optimal Dosage for the Efficacy of Submucosal Midazolam Administration to Induce Sedation in Children Undergoing Diagnostic Procedures

Esfahan University of Medical Sciences0 sites99 target enrollmentStarted: TBDLast updated:

Overview

Phase
Phase 2
Status
Recruiting
Enrollment
99

Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
3 months to 5 years (—)
Sex
All

Inclusion Criteria

  • The age range of over three months up to five years
  • Children requiring diagnostic procedures such as CT scan

Exclusion Criteria

  • The patients with excessive sensitivity to Benzodiazepines
  • Medical disorder of shock or blood pressure
  • Alcohol intoxication
  • Poor vital signs
  • Pulmonary diseases
  • Myasthenia gravis or musculoskeletal disorders

Investigators

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