Ignite Creation Date:
2024-05-06 @ 2:11 AM
Last Modification Date:
2024-10-26 @ 11:14 AM
Study NCT ID:
NCT01984853
Status:
COMPLETED
Last Update Posted:
2015-07-31
First Post:
2013-10-30
Brief Title:
Cardiology-Emergency Medicine Cardiac Biomarker Research Initiative
Sponsor:
Organization:
Henry Ford Health System
Study Design
Study Type:
OBSERVATIONAL
Expanded Access Type Individual:
None
Expanded Access Type Intermediate:
None
Expanded Access Type Treatment:
None
Patient Registry:
True
Target Duration:
18 Months
Design Allocation:
Design Intervention Model:
Design Intervention Model Description:
Design Masking Description:
Bio Spec Retention:
SAMPLES_WITHOUT_DNA
Bio Spec Description:
Approximately 6-85 ml of blood will be collected in each of two anticoagulant tube types SST and K2EDTA plasma
The first blood collection in the ED is designated as t0 ED ECG time 60 minutes
Additional blood draws of approximately 6-85 mLtube type will occur at t1 30 - 10 minutes after t0 t21 -15 minutes hour after t0 t4 3 - 15 minutes hours after t0 if the patient is still in the EDhospital
Enrollment Count:
575
Enrollment Type:
ACTUAL
Design Primary Purpose:
Design Masking:
Phases:
Observational Models:
| Name |
|---|
| Cohort |
Time Perspective List:
Clinical Trial Statuses
| Name |
|---|
| 23398 |
Who Masked List: