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Extracorporeal Membrane Oxygenation Effect in Prolonged Cardiopulmonary Resuscitation

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00173615
First Posted: September 15, 2005
Last Update Posted: January 19, 2009
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
National Taiwan University Hospital
  Purpose
Analysis of the patients' data who were rescued with extracorporeal membrane oxygenation and without ECMO. The survival rate and the weaning rate were analyzed to see the effect of ECMO on the prolonged CPR.

Condition Intervention
Cardiopulmonary Resuscitation Cardiac Arrest Ventricular Tachycardia Ventricular Fibrillation Procedure: Extracorporeal membrane oxygenation

Study Type: Observational

Resource links provided by NLM:


Further study details as provided by National Taiwan University Hospital:

Estimated Enrollment: 100
Study Start Date: April 1996
Study Completion Date: December 2006
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 85 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • CPR > 10 min without return of spontaneous circulation

Exclusion Criteria:

  • CPR with traumatic origin unless bleeding was under control, previous irreversible brain damage, terminal status of malignancy, and the age over 75 years. For the patients with post-cardiotomy shock requiring ECLS in the operating theater because of an inability of weaning from cardiopulmonary bypass, they were excluded as well from this ECPR cohort since they did not receive cardiac massage. The patients that had signed "Do-Not-Resuscitate" (DNR) consent were also excluded from ECLS deployment.
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00173615


Locations
Taiwan
National Taiwan University Hospital
Taipei, Taiwan, 100
Sponsors and Collaborators
National Taiwan University Hospital
Investigators
Principal Investigator: Yih-Sharng Chen, MD, PhD National Taiwan University Hospital
  More Information

Publications:

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
ClinicalTrials.gov Identifier: NCT00173615     History of Changes
Other Study ID Numbers: 9461700820
First Submitted: September 12, 2005
First Posted: September 15, 2005
Last Update Posted: January 19, 2009
Last Verified: January 2009

Keywords provided by National Taiwan University Hospital:
ECMO
CPR

Additional relevant MeSH terms:
Heart Arrest
Tachycardia
Tachycardia, Ventricular
Ventricular Fibrillation
Heart Diseases
Cardiovascular Diseases
Arrhythmias, Cardiac
Pathologic Processes