Clinical Trials Directory

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UnknownNCT01595399

Atropine Versus no Atropine for Neonatal Rapid Sequence Intubation

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
70 (estimated)
Sponsor
University of Manitoba · Academic / Other
Sex
All
Age
1 Day – 2 Months
Healthy volunteers
Not accepted

Summary

The purpose of this study is to compare heart rate in infants who receive atropine as a part of their medication before intubation to those who do not. To be able to find out , we need to divided babies into 2 groups; group 1 : receives atropine + sedation + muscle relaxant group 2 : receives water or saline ( placebo group) + sedation + muscle relaxant Then we need to compare heart rate during intubation and duration of intubation between the 2 groups.

Detailed description

We hypothesize that premedication for intubation with fentanyl and succinylcholine alone will maintain equal stability of heart rate and oxygen saturation without a prolongation of time to completion of intubation when compared to a protocol using atropine, fentanyl and succinylcholine. In order to answer this question we plan to undertake a prospective randomized double blinded control trial of use of atropine as an adjunct for elective intubation of infants less than 46 weeks postmenstrual age.

Conditions

Interventions

TypeNameDescription
DRUGatropineAtropine 0.02 mg/kg IV
DRUGPlaceboan equivalent volume of normal saline to atropine IV

Timeline

Start date
2012-04-01
Primary completion
2014-06-01
Completion
2014-06-01
First posted
2012-05-10
Last updated
2013-09-24

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT01595399. Inclusion in this directory is not an endorsement.