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Tracking Information | |||||
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First Received Date † | March 28, 2006 | ||||
Last Updated Date | March 28, 2006 | ||||
Start Date † | January 2005 | ||||
Current Primary Outcome Measures † |
Quality of CPR | ||||
Original Primary Outcome Measures † | Same as current | ||||
Change History | No Changes Posted | ||||
Current Secondary Outcome Measures † |
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Original Secondary Outcome Measures † | Same as current | ||||
Descriptive Information | |||||
Brief Title † | Comparison of Manual Cardiopulmonary Resuscitation (CPR) Versus Automatic CPR Machine During Ambulance Transport. | ||||
Official Title † | Comparison of Manual Cardiopulmonary Resuscitation (CPR) Versus Automatic CPR Machine on the CPR Performance for Out-of-Hospital Cardiac Arrest During Ambulance Transport. | ||||
Brief Summary | This is a randomized controlled prospective study which assigned patient to receive manual CPR or automatic CPR machine use. The quality and efficacy between manual CPR and machine CPR will be evaluated. |
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Detailed Description | |||||
Study Phase | |||||
Study Type † | Interventional | ||||
Study Design † | Treatment, Randomized, Single Blind, Active Control, Single Group Assignment, Safety/Efficacy Study | ||||
Condition † |
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Intervention † | Device: Automatic CPR machine | ||||
Study Arms / Comparison Groups | |||||
Publications * | |||||
* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline. |
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Recruitment Information | |||||
Recruitment Status † | Recruiting | ||||
Enrollment † | 100 | ||||
Completion Date | |||||
Primary Completion Date | |||||
Eligibility Criteria † | Inclusion Criteria:
Exclusion Criteria:
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Gender | Both | ||||
Ages | 16 Years and older | ||||
Accepts Healthy Volunteers | No | ||||
Contacts †† | |||||
Location Countries † | Taiwan | ||||
Expanded Access Status | |||||
Administrative Information | |||||
NCT ID † | NCT00308815 | ||||
Responsible Party | |||||
Secondary IDs †† | |||||
Study Sponsor † | National Taiwan University Hospital | ||||
Collaborators †† | |||||
Investigators † |
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Information Provided By | National Taiwan University Hospital | ||||
Verification Date | October 2004 | ||||
† Required WHO trial registration data element. †† WHO trial registration data element that is required only if it exists. |