Status:
COMPLETED
In Vivo PET of Synaptic Density in Cognitive Disorders
Lead Sponsor:
Universitaire Ziekenhuizen KU Leuven
Conditions:
Alzheimer Disease
Frontotemporal Degeneration
Eligibility:
All Genders
18+ years
Brief Summary
This study will compare the discriminative power of \[18F\]-SynVesT-1 PET and the standard-of-care \[18F\]-FDG PET in different cognitive disorders (Alzheimer's disease, Frontotemporal degeneration, d...
Detailed Description
Forty healthy controls will be included as well as 110 patients that were referred by the UZ Leuven memory clinic with uncertain diagnosis of cognitive impairment and are already sent for \[18F\]-FDG ...
Eligibility Criteria
Inclusion
- Healthy controls:
- Age between 18 and 85 years old (aimed to be evenly spread over age intervals).
- Subject is judged to be in good health by the investigator on the basis of medical history, physical examination including vital signs, clinical laboratory test and urinalysis.
- No history or evidence of current major neurological, internal or psychiatric disorder, based on the medical assessment and neuropsychological assessment.
- In subjects \< 60 years of age, an unremarkable structural MRI scan as assessed by expert radiologist. In subjects \>= 60 years of age white matter hyperintensities corresponding to a white matter lesion (WML) score \<= 2 (of 3) on the Age-Related White Matter changes scale are acceptable.
- When older than 50 years of age, subject is willing to undergo an additional 18F-NAV-4694 scan when cerebral amyloid status is unknown.
Exclusion
- Subject has a history of any major disease that may interfere with the investigations or make the subject unfit for participation according to the interpretation by the investigator (especially liver and kidney disease, uncontrolled diabetes or most forms of cancer).
- Subject has any history of a major neurological disorder or known cerebral structural abnormalities.
- Subject is first-degree relative (sibling, parent or children) of a person with neurological or psychiatric history assessed by a neurologist or psychiatrist (in particular dementia).
- Evidence of cognitive impairment as assessed by a MMSE score \< 28.
- Subject has a history or evidence of psychiatric disease, as assessed by a validated psychiatric symptom self-assessment tool (Symptom Checklist-90, Beck Depression Inventory (BDI) and Geriatric Depression Scale (GDS)).
- Subject is currently a user (including ''recreational use'') of any illicit drugs, including cannabis, or has a history of drug or alcohol abuse.
- Subject chronically uses medication that has central nervous system effects (e.g., opioids, neuroleptics, sedatives, anti-depressants, sleep medication).
- Subject has had exposure to ionizing radiation (\> 1 mSv) in other research studies within the last 12 months.
- Subject has a contra-indication for MRI scanning.
- Subject suffers from claustrophobia or cannot tolerate confinement during PET-MRI scanning procedures; subject cannot lie still for approximately 90 minutes inside the scanner.
- Subject is unwilling to avoid unusual, unaccustomed, or strenuous physical activity (i.e., weightlifting, running, bicycling) from the time of the pre-study visit until the end of scanning.
- Subject does not understand the study procedures.
- Subject is unwilling or unable to perform all of the study procedures or is considered unsuitable in any way by the principal investigator.
- Subject is pregnant (according to Ulti Med hCG urine test) or breastfeeding.
- Subject is a woman of childbearing potential (WOCBP) who does not agree to apply appropriate contraception methods during study participation and continues to do so for at least 6 months after study completion. For WOCBP: contraception methods with a relatively high Pearl index (natural methods, minipill outside postpartum period, spermicides or condoms in monotherapy or no usage of contraception when sexually active) are not accepted.
- Subject is a man with a pregnant or non-pregnant WOCBP partner, who does not agree to use a condom and continue to do so until 90 days after study completion. In addition, the non-pregnant WOCBP partner should use a highly effective method of contraception.
- Subject does not agree that incidental findings are communicated to the general practitioner and to the participant him/herself.
- Subject is on anticoagulant therapy.
- Patients:
- Inclusion Criteria:
- Patients referred with uncertain diagnosis and subsequent need for FDG PET brain in their work- up to differentiate between dementing disorders or to exclude dementia in late-onset psychiatric disorders with cognitive impairment.
- A routine neuropsychological assessment has been performed during clinical work-up in the memory clinic.
- Subject is at least 30 years old.
Key Trial Info
Start Date :
April 11 2022
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
June 4 2025
Estimated Enrollment :
134 Patients enrolled
Trial Details
Trial ID
NCT05384353
Start Date
April 11 2022
End Date
June 4 2025
Last Update
January 8 2026
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
UZ Leuven
Leuven, Belgium, 3000