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RECRUITING
NCT05677880

Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL) Study

Sponsor: University of Wisconsin, Madison

View on ClinicalTrials.gov

Summary

This is an observational study to better understand the risk factors and progression of CADASIL, a leading cause of vascular cognitive impairment and dementia (VCID). 575 participants will be enrolled and can expect to be on study for up to 5 years.

Official title: Unraveling the Early Phases of Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL)

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

660

Start Date

2022-06-03

Completion Date

2027-08

Last Updated

2026-01-15

Healthy Volunteers

Yes

Conditions

Interventions

OTHER

Study Procedures

Participants will experience * Neurocognitive Tests and Self-Report Measures * Clinical Interviews * Neurological Exam * MRI screening at baseline, 18 months, 36 months * Fasted Blood draw

Locations (12)

University of California

Los Angeles, California, United States

University of California

San Francisco, California, United States

University of Colorado

Denver, Colorado, United States

Georgia State University Research Foundation

Atlanta, Georgia, United States

Loyola University

Chicago, Illinois, United States

Columbia University

New York, New York, United States

Oregon Health & Science University

Portland, Oregon, United States

Brown University

Providence, Rhode Island, United States

University of Texas Health Science Center

Houston, Texas, United States

University of Texas

San Antonio, Texas, United States

University of Utah

Salt Lake City, Utah, United States

University of Washington

Seattle, Washington, United States