Stroke Thrombectomy and Aneurysm Registry
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Stroke/Thrombectomy/Aneurysm-specific surgical procedures.
- Who it may be relevant to
- Registry conditions: Stroke, Thromboses, Intracranial, Aneurysm, Brain. Basic parameters: 1 year — 120 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States, Canada, Germany, Japan, Portugal +4
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Overview
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.
Interventions
- Procedure Stroke/Thrombectomy/Aneurysm-specific surgical procedures
Participants are retrospectively and/or prospectively entered into registry based on disease indication and respective surgical procedure.
Primary outcome measures
- Post-procedure hemorrhage rate changes [Time frame: 90 days]
- Occlusion rates [Time frame: 90 days]
- Complication rates [Time frame: 90 days]
- Retreatment rates [Time frame: 90 days]
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
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
United States · 54 centers
- University of Alabama at Birmingham — Birmingham
- Loma Linda University — Loma Linda
- Cottage Health Research Institute — Santa Barbara
- Nuvance Health — Danbury
- Yale University — New Haven
- University of Florida — Gainesville
- Mayo Clinic in Florida — Jacksonville
- University of Miami Health System — Miami
- … and 46 more centers
Germany · 2 centers
- Universitätsmedizin Göttingen — Göttingen
- University Clinic for Neuroradiology — Magdeburg
Canada · 1 center
- University of Saskatchewan — Saskatoon
Japan · 1 center
- Hyogo College of Medicine — Hyōgo
Portugal · 1 center
- Centro Hospitalar Universitário de Lisboa Central — Lisbon
South Korea · 1 center
- Chonnam National University Hospital — Gwangju
Spain · 1 center
- Hospital Universitario La Paz — Madrid
Switzerland · 1 center
- Universitätsspital Basel — Basel
Uruguay · 1 center
- Médica Uruguaya — Montevideo
Identifiers
NCT: NCT04994756 · Pro00090704