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Pilot Study for Sedation Interruption in Children

NCT02426320 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2015-04-24

No results posted yet for this study

Summary

The purpose of this study is to estimate the hypothesized benefit of sedation interruption protocol on mechanical ventilation duration and PICU length of stay. The study will evaluate recruitment rates, and adherence rates of such protocol.

Conditions

  • Daily Sedative Interruption
  • Sedation Strategies
  • Sedation Protocols
  • Mechanical Ventilation
  • Sedation

Interventions

OTHER

Sedation Interruption Protocol

OTHER

Standard Sedation Protocol

Sponsors & Collaborators

  • Davinia Withington

    lead OTHER

Principal Investigators

  • Conall Francoeur · McGill University Health Centre/Research Institute of the McGill University Health Centre

  • Christina Maratta · McGill University Health Centre/Research Institute of the McGill University Health Centre

  • Maryse Dagenais · McGill University Health Centre/Research Institute of the McGill University Health Centre

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Max Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-04-30
Primary Completion
2015-04-30
Completion
2015-06-30

Countries

  • Canada

Study Locations

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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 NCT02426320 on ClinicalTrials.gov