NCT Number: NCT01786460
Brain Injury Biomarkers in the General Population
The purpose of this study is to use an investigational assay to assess levels of putative biomarkers of traumatic brain injury (TBI) in a general population. The data will be used in a correlative analysis with data collected under a separate study of severe TBI.
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Notify MeKey information
Conditions
Age range
18 year–80 year
Sex eligibility
All sexes
Study type
Observational
Primary location
Office of Nagi S. Ibrahim, Vista, California, United States
Who can participate
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- At least 18 years of age and no more than 80 years of age
- Willing to undergo consent
- PI believes volunteer is appropriate candidate for study
Exclusion criteria
- Participating in another clinical study that may affect the results of either study
- Non-English speaking
- Venipuncture not feasible
- Blood donation within 1 week of screening
- PI determines volunteer is not medically suitable for study participation
Treatment and study plan
Primary outcomes
-
Assessment of the putative biomarkers for TBI markers in general population using an investigational assay
Time frame: up to 21 days
Secondary outcomes
-
Correlation of the putative biomarkers for TBI levels in general population to levels in patients with severe TBI
Time frame: 0, 14, 7, and 21 days
Sponsors and collaborators
Lead sponsor
Banyan Biomarkers, Inc
Industry
Registry information
Important dates
- Study start
- 2011
- Primary completion
- 2011
- Study completion
- 2011
- First posted
- Feb 8, 2013
- Registry last updated
- Jan 31, 2017
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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