Actively Recruiting
InRAD Observational Study
Led by Stichting International Registry for Alzheimer's Disease and other Dementias Foundation · Updated on 2026-04-16
50000
Participants Needed
1
Research Sites
509 weeks
Total Duration
On this page
Sponsors
S
Stichting International Registry for Alzheimer's Disease and other Dementias Foundation
Lead Sponsor
I
InRAD Foundation (Data Processor)
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this international observational study is to evaluate long-term disease outcomes and treatment safety in people with Alzheimer's disease (PwAD), by collecting real-world data from routine clinical practice across global clinical centers. The InRAD Registry Observational Study has several aims: * To collect medical information for many years from a large group of people with Alzheimer's disease. This will be used for research, which will support improved understanding about the disease. * To enable researchers to look at the effectiveness, usefulness and safety of treatments for Alzheimer's disease. * To enable researchers to answer similar research questions and compare results in many different areas of the world. People with Alzheimer's disease who meet the eligibility criteria and agree to participate in the Study will be asked to visit their doctor (e.g. psychiatrist, geriatrician, or neurologist) at least once a year, or as frequently as is needed for their care. During or after their appointments they may be offered assessments, tests, medications, and treatments as determined by their doctor and their team. This is an observational data collection.
CONDITIONS
Official Title
InRAD Observational Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Undergoing diagnostic work-up for Alzheimer's disease or
- Have a confirmed diagnosis of Alzheimer's disease (treated or untreated)
- Attending an InRAD Center
- Provided informed consent for long-term follow-up
You will not qualify if you...
- Unable or unwilling to provide signed informed consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
UZLeuven
Leuven, Belgium, 3000
Actively Recruiting
Research Team
S
Scientific Officer
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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