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Search / Trial NCT05089331

ROSE-Longitudinal Assessment With Neuroimaging

Launched by STATE UNIVERSITY OF NEW YORK AT BUFFALO · Oct 11, 2021

Trial Information

Current as of July 22, 2025

Recruiting

Keywords

Hemorrhagic Stroke, Intracerebral Intracerebral Hemorrhage Outcomes After Stroke Intracerebral Hematoma

ClinConnect Summary

The ROSE-Longitudinal Assessment With Neuroimaging trial is studying how patients recover after experiencing a type of stroke called intracerebral hemorrhage, which involves bleeding within the brain. Researchers will follow up with 250 participants from an earlier study to see how their brain function and abilities, such as thinking and movement, change over time. This will take place 12 to 24 months after the stroke, with evaluations happening at various points to identify factors that may help predict recovery or ongoing challenges.

To be eligible for this trial, participants must be at least 18 years old and have had a specific type of intracerebral hemorrhage without any other complications like brain tumors or serious injuries. Participants will undergo advanced brain imaging and assessments of their cognitive and motor skills. The study aims to gather important information that could help doctors better understand how to support recovery in stroke patients. This trial is significant because it represents one of the largest studies of its kind, focusing on long-term brain health after a stroke.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • 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
  • Exclusion Criteria:
  • Brainstem or Cerebellar ICH
  • Patients Severely Affected by the ICH, Early Mortality, Hospice, or Withdraw of Care NOT eligible for ROS

About State University Of New York At Buffalo

The State University of New York at Buffalo (SUNY Buffalo) is a prominent research institution dedicated to advancing healthcare through innovative clinical trials and studies. Renowned for its commitment to academic excellence and interdisciplinary collaboration, the university leverages its extensive resources and expertise to explore novel therapeutic approaches and enhance patient outcomes. SUNY Buffalo's clinical trials encompass a wide range of medical disciplines, driven by a mission to translate research discoveries into practical applications that benefit diverse populations. With a focus on ethical standards and rigorous methodologies, the university fosters an environment that supports cutting-edge research while prioritizing participant safety and well-being.

Locations

New York, New York, United States

Baltimore, Maryland, United States

New York, New York, United States

Cincinnati, Ohio, United States

Durham, North Carolina, United States

Louisville, Kentucky, United States

Chicago, Illinois, United States

Houston, Texas, United States

Patients applied

0 patients applied

Trial Officials

Daniel Woo, MD, MS

Principal Investigator

State University of New York at Buffalo

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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