Actively Recruiting

Age: 18Years +
All Genders
NCT05089331

ROSE-Longitudinal Assessment With Neuroimaging

Led by State University of New York at Buffalo · Updated on 2025-07-04

250

Participants Needed

7

Research Sites

295 weeks

Total Duration

On this page

Sponsors

S

State University of New York at Buffalo

Lead Sponsor

N

National Institute of Neurological Disorders and Stroke (NINDS)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The investigators will perform follow-up on 250 of 500 cases recruited into the ROSE study of cases with deep and lobar intracerebral hemorrhage to perform advanced neuroimaging at 12-24 months post stroke, and evaluations of motor and cognitive function at baseline, 6 months after baseline, and 12 months after baseline to determine predictors of recovery, progressive cognitive or functional impairment. The investigators propose to leverage the recruitment, DNA, RNA-seq and baseline advanced neuroimaging cohort of ROSE to obtain long-term neuroimaging and identical assessments longitudinally to address critical questions regarding the progressive decline of patients 12 to 24 months post intracerebral hemorrhage (ICH) with long term cognitive follow-up to 36 months on average. This proposal would represent the largest, and longest advanced neuroimaging and RNA-sequencing evaluation after ICH to date.

CONDITIONS

Official Title

ROSE-Longitudinal Assessment With Neuroimaging

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or greater, fulfillment of the criteria for Deep, Subcortical or Lobar Intracerebral Hemorrhage
  • No evidence of trauma, vascular malformation or aneurysm, or brain tumor as a cause of ICH
  • Ability of the patient or legal representative to provide informed consent
Not Eligible

You will not qualify if you...

  • Brainstem or Cerebellar ICH
  • Patients severely affected by the ICH, early mortality, hospice, or withdrawal of care not eligible for ROSE

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 7 locations

1

University of Illinois Chicago

Chicago, Illinois, United States, 60612

Actively Recruiting

2

Baptist Health Louisville

Louisville, Kentucky, United States, 40207

Actively Recruiting

3

University of Maryland

Baltimore, Maryland, United States, 21201

Actively Recruiting

4

Columbia University

New York, New York, United States, 10032

Actively Recruiting

5

Duke University

Durham, North Carolina, United States, 27710

Actively Recruiting

6

University of Cincinnati

Cincinnati, Ohio, United States, 45267

Actively Recruiting

7

Houston Methodist

Houston, Texas, United States, 77030

Actively Recruiting

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Research Team

L

Lee A Gilkerson, RN, BSN

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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ROSE-Longitudinal Assessment With Neuroimaging | DecenTrialz