A Cohort Study on Thrombectomy for Stroke
Registrated Cohort Study on Thrombectomy for Stroke
1 other identifier
observational
300
1 country
1
Brief Summary
The cerebral collateral circulation refers to the subsidiary network of vascular channels that stabilize cerebral blood flow when principal conduits fail. Collateral status differs among patients with acute ischemic stroke. Relatively sparse attention has been devoted to the role of baseline collateral circulation in patients with acute ischemic stroke who are candidates for revascularization. This study aim to investigate the correlation between baseline collateral circulation and the likelihood of opening of an arterial occlusion, the extent of reperfusion, tissue injury and clinical impairment.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Nov 2020
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
November 15, 2020
CompletedStudy Start
First participant enrolled
November 15, 2020
CompletedFirst Posted
Study publicly available on registry
November 19, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 30, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 30, 2025
CompletedDecember 29, 2021
November 1, 2021
5.1 years
November 15, 2020
December 27, 2021
Conditions
Outcome Measures
Primary Outcomes (1)
Modified Rankin Scale
Good functional outcome will be defined by a Modified Rankin Scale of 0-2, 3 months after stroke onset
3 month
Eligibility Criteria
Patients experiencing brain infarction complicating the large-vessel occlusion
You may qualify if:
- Age ≥ 18 years.
- Mechanical thrombectomy initiated within 24 hours after onset
- CT perfusion can be performed before the initiation of thrombectomy and 24h after thrombectomy
You may not qualify if:
- Contraindication to imaging with contrast agents
- Delay between imaging and beginning of thrombectomy \> 90 minutes
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Department of Neurology, First Affiliated Hospital of Fujian Medical University
Fuzhou, 350000, China
Biospecimen
10mL venous blood sample will be collected Each participant
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Director of Neurology department
Study Record Dates
First Submitted
November 15, 2020
First Posted
November 19, 2020
Study Start
November 15, 2020
Primary Completion
December 30, 2025
Study Completion
December 30, 2025
Last Updated
December 29, 2021
Record last verified: 2021-11