Clinical trial Recruiting at 5 sites Observational Ages 18 and up

Genetic and environmental causes of hemorrhagic stroke

Official title: Genetic and Environmental Risk Factors for Hemorrhagic Stroke

Run by State University of New York at Buffalo · NCT00682695 · Data updated 2026-11-12

We will test whether specific genetic variants and environmental factors are linked to the risk of intracerebral hemorrhage in adults.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment1000 (estimated)
SponsorState University of New York at Buffalo
Academic / other
Locations7 sites (Chicago, Illinois and 6 other locations)
StatusRecruiting
StartedJanuary 1, 2025
Main results expectedDecember 31, 2029
Study endsDecember 31, 2029
Registry record updatedJuly 2, 2026
Trial IDNCT00682695 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults (18+) who are residents at the recruitment center for at least six months and either have had a spontaneous non-traumatic intracerebral hemorrhage or are enrolled as control participants willing to provide blood and clinical information.

Probably not a fit

People with hemorrhages caused by trauma, brain tumor/metastases, or infection, those unable to consent, or people seeking direct therapeutic benefit are unlikely to benefit from this observational genetic study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study will perform deep DNA sequencing and gene expression analysis focused on the 1q22 genomic region to find genetic contributors to non-lobar intracerebral hemorrhage (ICH). The team will recruit about 500 non-lobar ICH cases (approximately 150 Black and 350 White) and 1,000 controls to correlate sequence variation with expression levels in the same samples. Findings will be replicated in larger datasets including thousands of additional ICH cases and CHARGE consortium participants with MRI white matter hyperintensity measurements. The work aims to link replicated GWAS signals to functional changes that may explain ICH risk and broader small vessel disease mechanisms.

Why it matters

Potential benefit: If successful, the results could identify people at higher genetic risk for ICH and point to new targets for prevention or therapy.

How similar studies have gone: Previous GWAS work identified a replicated association at 1q22 that this study builds on, but deep sequencing and linked expression analyses at this locus remain less tested.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Age 18 or older
* Resident (6 months or longer) within the recruitment center
* Fulfillment of the criteria for spontaneous ICH
* No evidence of trauma, brain tumor/metastases or infectious processes as a cause of the hemorrhage
* Ability of the patient or legal representative to provide consent for an interview, blood pressure determinations and DNA sampling

Exclusion Criteria:

* N/A

Where it's running

  • Baptist Health Louisville
    Louisville, Kentucky, United States
    Recruiting
  • University of Maryland
    Baltimore, Maryland, United States
    Recruiting
  • Massachusetts General Hospital
    Boston, Massachusetts, United States
    Recruiting
  • Duke University
    Durham, North Carolina, United States
    Recruiting
  • University of Cincinnati
    Cincinnati, Ohio, United States
    Recruiting
  • University of Illinois Chicago
    Chicago, Illinois, United States
    Not yet recruiting
Show 1 more location
  • Columbia University
    New York, New York, United States
    Not yet recruiting

Study contacts

  • Principal investigator: Daniel Woo, MD — University of Cincinnati
  • Study coordinator: Lee A Gilkerson, RN, BSN
  • Email: Lee.gilkerson@uc.edu
  • Phone: 513-558-6140

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.