18F-AV-1451 and Florbetapir F 18 PET (Positron Emission Tomography) Imaging in Subjects at Risk for Chronic Traumatic Encephalopathy
Completed · Phase 2
Conditions studied: Chronic Traumatic Encephalopathy
In brief
This study will explore the use of flortaucipir as a biomarker for chronic traumatic encephalopathy (CTE) and examine the relationship between clinical presentation and tau deposition.
Key facts
- Study ID
- NCT02079766
- Run by
- Avid Radiopharmaceuticals
- People needed
- 41
- Starts
- 2014-06-01
- Expected to finish
- 2015-10-01
- Last updated by the study team
- 2020-09-07
Who can join
Age: any. Sex: male. Healthy volunteers: accepted.
You may qualify if…
- Male subjects consented and currently enrolled in the Diagnosing and Evaluating Traumatic Encephalopathy Using Clinical Tests (DETECT) or the Long-Term Consequences of Repetitive Brain Injury in Athletes study protocols
- Can tolerate up to two PET imaging sessions
- Have the ability to provide informed consent for study procedures
You may not qualify if…
- Claustrophobia
- Current clinically significant cardiovascular disease or clinically significant abnormalities on screening ECG
- History of risk factors for Torsades de Pointes or are taking drugs known to cause QT-prolongation
- Current clinically significant infectious disease, endocrine or metabolic disease, pulmonary, renal or hepatic impairment, or cancer that the investigator believes would affect study participation or scan results
- Have had a non-study related radiopharmaceutical imaging or treatment within 7 days prior to study PET imaging sessions
Where it is running
- Banner Alzheimer's Institute — Phoenix, Arizona, United States
- Boston University — Boston, Massachusetts, United States
Full record on ClinicalTrials.gov
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