Ignite Creation Date:
2024-05-06 @ 6:41 PM
Last Modification Date:
2024-10-26 @ 2:53 PM
Study NCT ID:
NCT05756426
Status:
RECRUITING
Last Update Posted:
2023-08-14
First Post:
2023-02-02
Brief Title:
Consortium for Optimized Integration of Bio-Artificial Blood Components for Adaptive Resuscitation Therapy
Sponsor:
Organization:
University of Maryland Baltimore
Study Design
Study Type:
OBSERVATIONAL
Expanded Access Type Individual:
None
Expanded Access Type Intermediate:
None
Expanded Access Type Treatment:
None
Patient Registry:
False
Target Duration:
None
Design Allocation:
Design Intervention Model:
Design Intervention Model Description:
Design Masking Description:
Bio Spec Retention:
SAMPLES_WITHOUT_DNA
Bio Spec Description:
Healthy Adult Volunteers Healthy volunteers can be any adult who meets eligibility criteria and is willing to donate blood for the purpose of this research study The individual will have 20 milliliters mL of blood drawn upon the time of consent The subject may donate up to 12 times maximum per year over the course of their enrollment no closer together than every 2 weeks 14 days Only basic demographic data will be collected ie Age Gender Ethnicity History of medical illness or Primary Diagnosis weight and current medicationstherapies The Informed Consent Form Documentation Checklist Specimen Collection Checklist will be utilized to ensure eligibility is checked and most recent Informed Consent Form ICF is signed prior to specimen collection
Enrollment Count:
250
Enrollment Type:
ESTIMATED
Design Primary Purpose:
Design Masking:
Phases:
Observational Models:
| Name |
|---|
| Cohort |
Time Perspective List:
Clinical Trial Statuses
| Name |
|---|
| 93149 |
Who Masked List: