Serial Measurement of a Plasma Stroke Biomarker Panel in Patients Undergoing Cardiac Surgery With Cardiopulmonary Bypass (Stroke08)
This study has been completed.
Sponsor:
Klinikum Ludwigshafen
Information provided by:
Klinikum Ludwigshafen
ClinicalTrials.gov Identifier:
NCT00812656
First received: December 19, 2008
Last updated: December 2, 2009
Last verified: December 2009
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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 ] [ Designated as safety issue: No ]
| 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| Ages Eligible for Study: | 18 Years and older (Adult, Senior) |
| Genders Eligible for Study: | Both |
| 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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Please refer to this study by its ClinicalTrials.gov identifier: NCT00812656
Please refer to this study by its ClinicalTrials.gov identifier: 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 |
| Study First Received: | December 19, 2008 |
| Last Updated: | December 2, 2009 |
| Health Authority: | Germany: Federal Institute for Drugs and Medical Devices |
ClinicalTrials.gov processed this record on September 28, 2016