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Recovery and Outcomes From Stroke

NCT04007757 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 500

Last updated 2025-07-04

No results posted yet for this study

Summary

The investigators will perform follow-up on 500 cases of deep and lobar intracerebral hemorrhage to perform advanced neuroimaging before 45 days post stroke, and evaluations of motor and cognitive function at baseline, 3 months and 6 months to determine predictors of recovery, progressive cognitive or functional impairment.

Conditions

  • Intracerebral Hemorrhage

Sponsors & Collaborators

  • National Institute of Neurological Disorders and Stroke (NINDS)

    collaborator NIH

  • Massachusetts General Hospital

    collaborator OTHER

  • University of Maryland, Baltimore

    collaborator OTHER

  • Duke University, Durham, NC

    collaborator UNKNOWN

  • Columbia University

    collaborator OTHER

  • University of Illinois at Chicago

    collaborator OTHER

  • Baptist Health, Louisville

    collaborator OTHER

  • The Methodist Hospital Research Institute

    collaborator OTHER

  • State University of New York at Buffalo

    lead OTHER

Principal Investigators

  • Daniel Woo, MD, MS · State University of New York at Buffalo

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-08-23
Primary Completion
2024-10-31
Completion
2024-10-31

Countries

  • United States

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04007757 on ClinicalTrials.gov