Vascular Aspects in Dementia: Part 2
Launched by LEIDEN UNIVERSITY MEDICAL CENTER · Mar 18, 2024
Trial Information
Current as of October 25, 2025
Recruiting
Keywords
ClinConnect Summary
The clinical trial titled "Vascular Aspects in Dementia: Part 2" is studying a condition called cerebral amyloid angiopathy (CAA), which is often found in people with Alzheimer's disease (AD). The main goal of the study is to understand how blood flow changes in the brain during different stages of Alzheimer's and how this might relate to the worsening of memory and thinking skills. Researchers will use a special type of MRI scan to observe these blood flow changes and see how they progress over time in both individuals with early-stage Alzheimer's and healthy individuals.
To participate in this study, you may be eligible if you are between 50 and 90 years old and can give informed consent. This includes people who have been diagnosed with Alzheimer's, mild cognitive impairment (MCI), or are healthy adults without memory issues. Participants can expect to undergo MRI scans and share information about their memory and health. It’s important to note that certain conditions, like having a pacemaker or severe physical restrictions, may prevent someone from participating. This research is a crucial step in finding better treatments for Alzheimer's disease by understanding how CAA might influence its progression.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • For this study three different routes for inclusion exists. Inclusion criteria for each group separately are shown below.
- • 1. Participants who were included in our previous CASCADE study (P19.039).
- • Capable of giving informed consent (see appendix)
- • 2. Patients who attended a memory clinic within one year ago
- • Diagnosed with (mixed) probable AD
- • Diagnosed as MCI
- • Diagnosed as SCI
- • Age between 50-90 years
- • Capable of giving informed consent (see appendix)
- • 3. Control subjects
- • Healthy adults without memory complaints
- • Age between 50 -90 years
- • Capable of giving informed consent
- Exclusion Criteria:
- * Contra-indication to MRI scanning:
- • Claustrophobia
- • Pacemakers and defibrillators
- • Nerve stimulators
- • Intracranial clips
- • Intraorbital or intraocular metallic fragments
- • Cochlear implants
- • Ferromagnetic implants
- • Hydrocephaluspump
- • Intra-utrine device (not all types) Permanent make-up
- • Tattoos above the shoulders (not all)
- • Specific contraindications to fMRI
- • Seizure within prior year.
- • Noncorrectable visual impairment.
- • MMSE \< 19 points (measured at moment of screening or at memory clinic with a maximum of 6 months in retrospect)
- • Severe physical restrictions (completely wheelchair dependent)
- • Age above 90
About Leiden University Medical Center
Leiden University Medical Center (LUMC) is a prominent academic medical center located in the Netherlands, renowned for its commitment to advancing healthcare through innovative research and high-quality patient care. As a clinical trial sponsor, LUMC focuses on translating scientific discoveries into effective therapies, fostering collaborations between researchers, clinicians, and industry partners. The center is dedicated to conducting rigorous clinical studies across various medical fields, ensuring adherence to ethical standards and regulatory requirements while prioritizing patient safety and outcomes. Through its multidisciplinary approach, LUMC aims to contribute significantly to the understanding and treatment of complex health conditions, driving progress in personalized medicine and improving global health.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Leiden, Zuid Holland, Netherlands
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported