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

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00812656
First Posted: December 22, 2008
Last Update Posted: December 3, 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:
Klinikum Ludwigshafen
  Purpose
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
Cardiac Surgery

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Serial Measurement of a Plasma Stroke Biomarker Panel in Patients Undergoing Cardiac Surgery With Cardiopulmonary Bypass

Resource links provided by NLM:


Further study details as provided by Klinikum Ludwigshafen:

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

Enrollment: 50
Study Start Date: December 2008
Study Completion Date: December 2009
Primary Completion Date: December 2009 (Final data collection date for primary outcome measure)
Groups/Cohorts
Stroke Panel group
Patients undergoing cardiac surgery with the use of cardiopulmonary bypass

  Eligibility

Information from the National Library of Medicine

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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
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

Responsible Party: Prof. Dr. J. Boldt, Klinikum Ludwigshafen
ClinicalTrials.gov Identifier: NCT00812656     History of Changes
Other Study ID Numbers: StrokePanel08
First Submitted: December 19, 2008
First Posted: December 22, 2008
Last Update Posted: December 3, 2009
Last Verified: December 2009