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Clinical Trials/NCT01402596
NCT01402596
Withdrawn
Phase 2

Evaluation of Pediatric Procedural Sedation With Rectal Chloral Hydrate or Intranasal Midazolam - a Randomized Controlled Trial

University of Sao Paulo1 site in 1 countryAugust 2011

Overview

Phase
Phase 2
Intervention
Chloral Hydrate
Conditions
Traumatic Brain Injury
Sponsor
University of Sao Paulo
Locations
1
Primary Endpoint
Adverse Events
Status
Withdrawn
Last Updated
12 years ago

Overview

Brief Summary

Thousands of children receive sedation for diagnostic and therapeutic interventions annually, and this number is expected to increase. Children are at higher risk for sedation-related complications than adults. In different scenarios, multiple drugs are used to achieve sedation, each one with particular adverse events that must be monitored and reported.

Children that need CT scans for traumatic brain injuries often need sedation, without needing and IV line for that. Chloral hydrate is an hypnotic agent used since 1832 with low incidence of adverse events; however, despite its worldwide use, it's being abandoned due to bitter taste, long time of sedation onset, vomiting and mild sedation. Intranasal midazolam, on the other hand, produces high and fast concentrations on CSF with greater rates of success but probably with higher adverse events. There are no prospective studies with large series of patients using intranasal midazolam.

The aim of this study is to determine if nasal midazolam is a safer approach and more effective sedative regimen when compared to rectal chloral hydrate to children undergoing CT scans.

Registry
clinicaltrials.gov
Start Date
August 2011
End Date
August 2012
Last Updated
12 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • children undergoing CT scanning for TBI

Exclusion Criteria

  • epistaxis
  • suspected or confirmed skull or nasal fracture
  • Moderate to severe traumatic brain injury
  • hemodynamically unstable

Arms & Interventions

Chloral hydrate

Children undergoing CT scanning will receive in this arm 50 mg per kg of rectal chloral hydrate.

Intervention: Chloral Hydrate

Midazolam

Children undergoing CT scanning will receive in this arm 0,4 mg/kg of nasal midazolam.

Intervention: Midazolam

Outcomes

Primary Outcomes

Adverse Events

Time Frame: Participants will be followed for the duration of hospital (emergency department) stay, an expected average of 2-3 hours

Such as hypoxemia, respiratory depression, vomiting, hypotension

Secondary Outcomes

  • Efficacy of both drugs(Participants will be followed for the duration of hospital (emergency department) stay, an expected average of 2-3 hours)

Study Sites (1)

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