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Stroke Thrombectomy and Aneurysm Registry

RecruitingObservational study

Who can join

Ages 1 to 120 · All sexes

Full eligibility criteria

Inclusion Criteria:

* Undergoing surgical intervention for central nervous system vascular lesion
* Between 1 and 120 years of age

Exclusion Criteria:

* No exclusion criteria

About the study

This international multi-center registry is used to collect existing information and outcomes for patients undergoing an operation for treatment of injuries to the brain including the blockage of blood flow to an area of the brain, an abnormal ballooning of an artery, abnormal tangling of blood vessels, abnormal formation of blood vessels, tearing of vein, and bleeding in the brain. This information is used to help predict outcomes that undergo an operation for treatment of the above-listed brain injuries. Additionally, the information is used to compare techniques and devices' effects on technical and clinical outcomes.

What is being tested

Stroke/Thrombectomy/Aneurysm-specific surgical procedures (procedure)

Sponsor: Medical University of South Carolina · Participants: 40,000 · Started: Sep 17, 2019

Contact the study team

Alejandro M Spiotta, MD · Phone: 843-792-9226
Meredith Robinson, MS · Phone: 843-792-3164

Official record on ClinicalTrials.gov — NCT04994756

Locations in the U.S.

Alabama	University of Alabama at Birmingham, Birmingham
California	Loma Linda University, Loma Linda Cottage Health Research Institute, Santa Barbara
Connecticut	Nuvance Health, Danbury Yale University, New Haven
Florida	University of Florida, Gainesville Mayo Clinic in Florida, Jacksonville University of Miami Health System, Miami University of South Florida, Tampa
Georgia	Emory University, Atlanta Piedmont Healthcare, Atlanta
Hawaii	The Queens Health Center, Honolulu
Illinois	Rush University, Chicago University of Chicago, Chicago University of Illinois, Chicago Endeavor Health, Evanston
Indiana	Indiana University, Indianapolis
Iowa	University of Iowa, Iowa City
Kansas	University of Kansas Medical Center, Kansas City
Kentucky	University of Louisville, Louisville
Louisiana	Tulane University, New Orleans Louisiana State University Health Shreveport, Shreveport
Massachusetts	Beth Israel Deaconess Medical Center, Boston
Michigan	University of Michigan, Ann Arbor University of Michigan Health-West, Wyoming
Minnesota	Mayo Clinic, Rochester
Missouri	Washington University in St. Louis, St Louis
New Hampshire	Portsmouth Regional Hospital, Portsmouth
New Jersey	Rutgers University, New Brunswick Global Neurosciences Institute, Pennington
New York	Albany Medical Center, Albany The Feinstein Institutes for Medical Research, Great Neck Stony Brook University, Stony Brook Montefiore Medical Center, The Bronx
North Carolina	University of North Carolina, Raleigh Wake Forest Baptist Health, Winston-Salem
Ohio	Mercy Health, Toledo
Oklahoma	University of Oklahoma, Oklahoma City
Pennsylvania	Thomas Jefferson University, Philadelphia Alleghany Hospital, Pittsburgh Geisinger Medical Group, Wilkes-Barre WellSpan York Hospital, York
South Carolina	Medical University of South Carolina, Charleston
Tennessee	University of Tennessee Health Science Center, Memphis
Texas	The University of Texas Medical Branch at Galveston, Galveston Valley Baptist Medical Center, Harlingen Baylor College of Medicine, Houston HCA Houston Healthcare Kingwood, Kingwood Texas Stroke Institute, Plano University of Texas Health Science Center at San Antonio, San Antonio
Utah	University of Utah, Salt Lake City
Virginia	University of Virginia, Charlottesville
Washington	University of Washington, Seattle
West Virginia	West Virginia University, Morgantown

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.