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Serial Measurement of a Plasma Stroke Biomarker Panel in Patients Undergoing Cardiac Surgery With Cardiopulmonary Bypass (Stroke08)

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ClinicalTrials.gov Identifier: NCT00812656
Recruitment Status : Completed
First Posted : December 22, 2008
Last Update Posted : December 3, 2009
Sponsor:
Information provided by:
Klinikum Ludwigshafen

Study Description
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Study Description Study Design Groups and Cohorts Outcome Measures Eligibility Criteria Contacts and Locations More Information
Brief Summary:
The purpose of this study is to investigate changes in new plasma stroke biomarker panel in patients undergoing cardiac surgery with the use of cardiopulmonary bypass.

Condition or disease
Cardiac Surgery

Study Design
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Study Type : Observational
Actual Enrollment : 50 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Serial Measurement of a Plasma Stroke Biomarker Panel in Patients Undergoing Cardiac Surgery With Cardiopulmonary Bypass
Study Start Date : December 2008
Actual Primary Completion Date : December 2009
Actual Study Completion Date : December 2009

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Heart Surgery
U.S. FDA Resources

Groups and Cohorts
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Study Description Study Design Groups and Cohorts Outcome Measures Eligibility Criteria Contacts and Locations More Information

Group/Cohort
Stroke Panel group
Patients undergoing cardiac surgery with the use of cardiopulmonary bypass


Outcome Measures
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Study Description Study Design Groups and Cohorts Outcome Measures Eligibility Criteria Contacts and Locations More Information

Primary Outcome Measures :
  1. Change in stroke index [ Time Frame: day before surgery; first and second day postoperatively ]

Eligibility Criteria
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Study Description Study Design Groups and Cohorts Outcome Measures Eligibility Criteria Contacts and Locations More Information

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
Adult patients undergoing cardiac surgery with the use of cardiopulmonary bypass
Criteria

Inclusion Criteria:

  • Age > 18 years
  • Elective cardiac surgery with the use of cardiopulmonary bypass

Exclusion Criteria:

  • Patients undergoing emergent procedures
  • Patients with preoperative mechanical support
Contacts and Locations
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Study Description Study Design Groups and Cohorts Outcome Measures Eligibility Criteria Contacts and Locations More Information

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): NCT00812656


Locations
Germany
Klinikum Ludwigshafen
Ludwigshafen, RLP, Germany, 67063
Sponsors and Collaborators
Klinikum Ludwigshafen
Investigators
Principal Investigator: Stefan W Suttner, MD Klinikum Ludwigshafen
More Information
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Study Description Study Design Groups and Cohorts Outcome Measures Eligibility Criteria Contacts and Locations More Information

Responsible Party: Prof. Dr. J. Boldt, Klinikum Ludwigshafen
ClinicalTrials.gov Identifier: NCT00812656     History of Changes
Other Study ID Numbers: StrokePanel08
First Posted: December 22, 2008    Key Record Dates
Last Update Posted: December 3, 2009
Last Verified: December 2009