Genetic Studies in Familial Dementia

NCT ID: NCT04680013

Last Updated: 2025-03-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

4884 participants

Study Classification

OBSERVATIONAL

Study Start Date

2007-06-01

Study Completion Date

2024-10-29

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The purpose of this study is to identify genetic factors that contribute to or cause dementia (loss of memory) and related disorders across all ages and ethnic groups. This includes a number of neurological diseases such as early and late-onset Alzheimer disease, mild cognitive impairment, and other dementias.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Dementia of Alzheimer Type Alzheimer Disease, Late Onset Alzheimer Disease, Early Onset Mild Cognitive Impairment Dementia

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Cognitive Control

Participants in this group are cognitively intact.

No interventions assigned to this group

Mild Cognitive Impairment

Participants in this group have mild cognitive impairment.

No interventions assigned to this group

Dementia Group

Participants in this group have dementia.

No interventions assigned to this group

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

1. 18 years and older
2. Patients diagnosed with dementia, their family members and unrelated healthy controls without dementia.

Exclusion Criteria

1\. Individuals with competing diagnosis such as: Amyotrophic lateral sclerosis, Frontotemporal lobar degeneration, Multiple system atrophy, Corticobasal degeneration, Progressive Supranuclear Palsy, Huntington's disease, traumatic brain injury, drug or alcohol abuse, or schizophrenia, etc. (unless family members of a dementia affected individual).
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Case Western Reserve University

OTHER

Sponsor Role collaborator

Columbia University

OTHER

Sponsor Role collaborator

Wake Forest University

OTHER

Sponsor Role collaborator

National Institute on Aging (NIA)

NIH

Sponsor Role collaborator

University of Miami

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Margaret Pericak-Vance

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Margaret Pericak-Vance, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Miami

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

University of Miami

Miami, Florida, United States

Site Status

Countries

Review the countries where the study has at least one active or historical site.

United States

Related Links

Access external resources that provide additional context or updates about the study.

http://www.niagads.org

NIA Genomics of Alzheimer Disease Storage site

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

RF1AG054080

Identifier Type: NIH

Identifier Source: secondary_id

View Link

RF1AG054074

Identifier Type: NIH

Identifier Source: secondary_id

View Link

U01AG052410

Identifier Type: NIH

Identifier Source: secondary_id

View Link

20070307

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Genetics of Motor Learning
NCT01105845 TERMINATED
Genetic Variants in Stroke
NCT07186517 NOT_YET_RECRUITING