Serial Measurement of a Plasma Stroke Biomarker Panel in Patients Undergoing Cardiac Surgery With Cardiopulmonary Bypass (Stroke08)
![]() |
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. |
ClinicalTrials.gov Identifier: NCT00812656 |
Recruitment Status
:
Completed
First Posted
: December 22, 2008
Last Update Posted
: December 3, 2009
|
- Study Details
- Tabular View
- No Results Posted
- Disclaimer
- How to Read a Study Record
Condition or disease |
---|
Cardiac Surgery |
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 |

Group/Cohort |
---|
Stroke Panel group
Patients undergoing cardiac surgery with the use of cardiopulmonary bypass
|
- Change in stroke index [ Time Frame: day before surgery; first and second day postoperatively ]

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
Ages Eligible for Study: | 18 Years and older (Adult, Senior) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Sampling Method: | Probability Sample |
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

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
Germany | |
Klinikum Ludwigshafen | |
Ludwigshafen, RLP, Germany, 67063 |
Principal Investigator: | Stefan W Suttner, MD | Klinikum Ludwigshafen |
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 |