Actively Recruiting

All Genders
NCT07213700

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

All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Trial Site Locations

Total: 1 location

1

UZLeuven

Leuven, Belgium, 3000

Actively Recruiting

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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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