PET Imaging of Cyclooxygenases in Dementia
-
- STATUS
- Recruiting
-
- participants needed
- 64
-
- sponsor
- National Institute of Mental Health (NIMH)
Summary
- Background
About 5 million adults in the U.S. have
- Objective
To learn if two new radiolabeled
- Eligibility
Adults age 18 years and older in good general health who have an adult-onset
neurodegenerative
- Design
Participants will be screened with medical history, physical exam with vital signs, and lab
Participants will have a
Participants will have 2
Participants will have 2-3 study visits. Participation lasts 1 week to 4 months, depending on scheduling.
Description
Study Description: This pilot/exploratory study will examine whether
Objectives: Primary Objective: To determine whether
Endpoints: Primary Endpoint: Measurement of
Study Population: Four groups of 16 subjects each will be studied: 1)
Phase: 1
Description of Sites/Facilities Enrolling Participants: Screening and
Description of Study Intervention:
Subjects will be intravenously injected with 20
Study Duration: 36 months
Participant Duration: One week to four months, depending on the patient s availability and
access to MRI and
Details
Condition |
|
---|---|
Age | 18years - 100years |
Treatment | 11C-MC1, 11C-PS13 |
Clinical Study Identifier | NCT04396873 |
Sponsor | National Institute of Mental Health ( |
Last Modified on | 19 February 2024 |
How to participate?
,
Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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