Trials / Unknown
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
| Type | Name | Description |
|---|---|---|
| DRUG | atropine | Atropine 0.02 mg/kg IV |
| DRUG | Placebo | an 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.