Time to Defibrillation Using Automated External Defibrillators by Pediatric Residents in Simulated Cardiac Arrests
This study has been completed.
Sponsor:
Baylor College of Medicine
Information provided by:
Baylor College of Medicine
ClinicalTrials.gov Identifier:
NCT00640354
First received: March 18, 2008
Last updated: NA
Last verified: March 2008
History: No changes posted
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Purpose
Automated external defibrillators have improved survival for adult in hospital cardiac arrest. Automated external defibrillators are approved for children aged 1 year and older for out of hospital cardiac arrests. It is unknown whether automated external defibrillators have a role for in hospital pediatric cardiac arrests.
The purpose of study is to compare the management of cardiac rhythm disorders by pediatric residents using an automated external defibrillator versus a standard defibrillator in simulated pediatric cardiac arrests.
It is our hypothesis that residents using an automated external defibrillator will have a shorter time to defibrillation.
| Condition | Intervention |
|---|---|
|
Pediatric Residents |
Device: Automated external defibrillator Device: Manual defibrillator |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Defibrillation by Automated External Defibrillators Versus Manual Defibrillators in Simulated Pediatric In-Hospital Cardiac Arrests: A Prospective Randomized Controlled Trial of Pediatric Residents |
Resource links provided by NLM:
Further study details as provided by Baylor College of Medicine:
Primary Outcome Measures:
- Time to defibrillation [ Time Frame: Within 5 minutes of the start of the simulated cardiac arrest ] [ Designated as safety issue: No ]
| Enrollment: | 60 |
| Study Start Date: | December 2006 |
| Study Completion Date: | February 2007 |
| Primary Completion Date: | February 2007 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: 1
Pediatric residents randomized to having an automated external defibrillator
|
Device: Automated external defibrillator
Residents randomized to this group had an automated external defibrillator available for the simulated cardiac arrest. The automated external defibrillator did not actually discharge energy into the simulated patient
|
|
Active Comparator: 2
Pediatric residents randomized to having a manual defibrillator
|
Device: Manual defibrillator
Residents randomized to this group had a manual defibrillator available for the simulated cardiac arrest. The defibrillator did not actually discharge energy into the simulated patient.
|
Eligibility| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Pediatric resident at Baylor College of Medicine
Exclusion Criteria:
- Not a pediatric resident at Baylor College of Medicine
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00640354
Locations
| United States, Texas | |
| Texas Children's Hospital | |
| Houston, Texas, United States, 77030 | |
Sponsors and Collaborators
Baylor College of Medicine
Investigators
| Principal Investigator: | Antonio R Mott, MD | Baylor College of Medicine |
More Information
Publications:
Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | Joseph Rossano / Cardiology Fellow, Baylor College of Medicine |
| ClinicalTrials.gov Identifier: | NCT00640354 History of Changes |
| Other Study ID Numbers: | H - 18876 |
| Study First Received: | March 18, 2008 |
| Last Updated: | March 18, 2008 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by Baylor College of Medicine:
|
Automated External Defibrillator Resuscitation Pediatric |
Additional relevant MeSH terms:
|
Heart Arrest Heart Diseases Cardiovascular Diseases |
ClinicalTrials.gov processed this record on June 18, 2013