Stroke Thrombectomy and Aneurysm Registry

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.

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Key information

Conditions

Stroke Aneurysm Aneurysm, Brain Brain Diseases Cardiovascular Diseases Central Nervous System Diseases Cerebrovascular Disorders Embolism and Thrombosis Intracranial Aneurysm Intracranial Arterial Diseases Intracranial Embolism and Thrombosis Intracranial Thrombosis Nervous System Diseases Thromboembolism Thromboses, Intracranial Vascular Diseases

Age range

1 year–120 year

Sex eligibility

All sexes

Study type

Observational

Primary location

University of Saskatchewan, Saskatoon, Canada

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

No exclusion criteria

Treatment and study plan

Stroke/Thrombectomy/Aneurysm-specific surgical procedures

Procedure

Participants are retrospectively and/or prospectively entered into registry based on disease indication and respective surgical procedure.

Primary outcomes

Post-procedure hemorrhage rate changes

Time frame: 90 days

Researchers examine changes in hemorrhage rates in post-stroke patients
Occlusion rates

Time frame: 90 days

Measure of how thrombectomy procedure success in relation to reduced occlusion
Complication rates

Time frame: 90 days

Measure of post-procedure complication rates in stroke/aneurysm patients
Retreatment rates

Time frame: 90 days

Measure of patient retreatment post-procedure

Study contacts

Contact information is provided by the study sponsor or research team.

Alejandro M Spiotta, MD

CONTACT

[email protected]

843-792-9226

Meredith Robinson, MS

CONTACT

[email protected]

843-792-3164

Sponsors and collaborators

Lead sponsor

Medical University of South Carolina

Other

Registry information

Acronym: STAR

Important dates

Study start: 2019
Primary completion: 2055
Study completion: 2055
First posted: Aug 6, 2021
Registry last updated: Dec 24, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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