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The International Registry for Alzheimer's Disease and Other Dementias (InRAD): An International Registry Observational Study Dedicated to Evaluating Outcomes Data in Alzheimer's Disease

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Observational
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Healthy Volunteers: f
View:

• Be undergoing diagnostic work-up for Alzheimer's disease (AD), OR

• Have a confirmed diagnosis of AD (whether currently treated with an AD-specific treatment, or untreated),

• Be attending an InRAD Center,

• Have provided informed consent for long-term follow-up

Locations
Other Locations
Belgium
UZLeuven
RECRUITING
Leuven
Contact Information
Primary
Scientific Officer
office@inradnetwork.org
Time Frame
Start Date: 2026-03-30
Estimated Completion Date: 2036-01
Participants
Target number of participants: 50000
Treatments
Alzheimer's Disease Registry Participants
Individuals diagnosed with Alzheimer's disease or undergoing diagnostic work-up, enrolled in the InRAD Registry for long-term observational follow-up. This cohort includes treated, treatment-eligible, and untreated patients across global clinical centers participating in routine care and data collection.
Related Therapeutic Areas
Sponsors
Collaborators: All Individual Principal Investigators and their centers (Data Controllers), InRAD Foundation (Data Processor)
Leads: Stichting International Registry for Alzheimer's Disease and other Dementias Foundation

This content was sourced from clinicaltrials.gov