Brain bleed survivors studied for clot Removal's Long-Term brain benefits
NCT ID NCT05611918
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This study follows 350 people who survived a brain bleed (intracerebral hemorrhage) and were part of earlier trials. Researchers will test memory, thinking, and movement skills over time, and collect blood samples to look for signs of ongoing inflammation. The goal is to see if surgically removing the clot helps prevent long-term cognitive decline.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this study could show that removing the clot after a brain bleed helps prevent memory and thinking problems later in life.
- What could go wrong
- This is an observational follow-up, not a new treatment trial. It cannot prove cause and effect, and results may not apply to all survivors.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 350 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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May 2023
- Expected to finish
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Dec 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
The study populations includes all surviving cases identified and recruited through the 5-year durations of the MISTIE III and ENRICH trials and with follow-up periods extending from 2013-2017 and 2016-2022, respectively.
- Ages
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Participants in the study must be survivors enrolled in MISTIE III and ENRICH trials at end of each trial's final follow-up (day 365 in MISTIE III and day 180 in ENRICH). Relatives of known survivors that are found to be deceased since the end of each trial will be interviewed to capture relevant data. Exclusion Criteria: * None
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Albert Einstein Montefiore
The Bronx, New York, 10461, United States
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CommonSpirit (formerly Mercy San Juan Medical Center; dignity health)
Chicago, Illinois, 60606, United States
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Dignity Health component - St. Joseph's Hospital and Medical Center
Sacramento, California, 95819, United States
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Hennepin Healthcare Research Institute
Minneapolis, Minnesota, 55415, United States
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Henry Ford Health System
Detroit, Michigan, 48202, United States
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Inova Health System Foundation
Fairfax, Virginia, 22042, United States
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Johns Hopkins Hospital
Baltimore, Maryland, 21205, United States
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Mayo Clinic, Jacksonville
Jacksonville, Florida, 32224, United States
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Rutgers - Robert Wood Johnson Medical School
Piscataway, New Jersey, 08854, United States
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Scripps Health
La Jolla, California, 92037, United States
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Stanford University
Stanford, California, 94305, United States
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Thomas Jefferson University
Philadelphia, Pennsylvania, 19107, United States
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University of Alabama at Brimingham
Birmingham, Alabama, 35294, United States
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University of Cincinnati
Cincinnati, Ohio, 45220, United States
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University of Illinois at Chicago
Chicago, Illinois, 60607, United States
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University of Kansas Medical Center
Fairway, Kansas, 66205, United States
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University of Louisville
Louisville, Kentucky, 40292, United States
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University of Maryland Baltimore
Baltimore, Maryland, 21201, United States
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University of Michigan
Ann Arbor, Michigan, 48109, United States
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University of New Mexico
Albuquerque, New Mexico, 87131, United States
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University of Texas Health Science Center at San Antonio
San Antonio, Texas, 78229, United States
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University of Texas, Houston Health Science Center
Houston, Texas, 77030, United States
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Vanderbilt University Medical Center
Nashville, Tennessee, 37232, United States
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Wake Forest University Health Sciences
Winston-Salem, North Carolina, 27157, United States
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Washington University in St. Louis, School of Medicine
St Louis, Missouri, 63130, United States
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Yale University
New Haven, Connecticut, 06511, United States
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Other studies related to the condition(s) this trial covers.
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