Inflammatory Markers and Prognosis After Cerebral Thrombectomy in Large Vessel Occlusion
IMPACT-LVO
Local-to-Systemic Inflammatory Biomarker Gradients and 90-Day Functional Outcomes in Patients With Acute Ischemic Stroke Due to Anterior Circulation Large Vessel Occlusion Undergoing Mechanical Thrombectomy: A Prospective Observational Cohort Study
1 other identifier
observational
50
1 country
1
Brief Summary
The goal of this observational study is to describe the local change in interleukin-6 (IL-6) across a blood clot in adults with acute ischemic stroke caused by anterior circulation large vessel occlusion who are undergoing mechanical thrombectomy. The main questions it aims to answer are:
- Is the level of IL-6 different in arterial blood collected beyond the clot compared with arterial blood collected before the clot during mechanical thrombectomy?
- Is the trans-thrombus IL-6 difference associated with functional independence 90 days after stroke and with complications related to reperfusion injury? There is no comparison group and no experimental treatment. Researchers will compare paired blood samples collected from opposite sides of the clot in the same participant. Blood collected from a peripheral vein at hospital admission will be used only as a supportive reference for systemic inflammation. Participants will:
- Receive standard mechanical thrombectomy and stroke care determined by their treating clinical team.
- Have small blood samples collected at planned time points, including paired arterial blood samples collected during the thrombectomy procedure.
- Have clinical and imaging information collected from their medical records and have functional status assessed 90 days after stroke. The study will not delay or change standard stroke treatment.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Aug 2026
Typical duration 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
Study Start
First participant enrolled
August 1, 2026
CompletedFirst Submitted
Initial submission to the registry
August 4, 2026
CompletedFirst Posted
Study publicly available on registry
August 10, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2028
ExpectedStudy Completion
Last participant's last visit for all outcomes
August 1, 2029
August 10, 2026
August 1, 2026
2 years
August 4, 2026
August 4, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Trans-Thrombus Interleukin-6 Gradient
The primary outcome is the within-participant trans-thrombus interleukin-6 (IL-6) gradient, defined as ln \[T2b/T2a\], where T2b is the IL-6 concentration in arterial plasma collected distal to the thrombus and T2a is the IL-6 concentration in arterial plasma collected proximal to the thrombus.
During mechanical thrombectomy, before recanalization
Secondary Outcomes (12)
Trans-Thrombus Interleukin-1 Beta Gradient
During mechanical thrombectomy, before recanalization
Trans-Thrombus Interleukin-17 Gradient
During mechanical thrombectomy, before recanalization
Trans-Thrombus Complement C3 Gradient
During mechanical thrombectomy, before recanalization
Trans-Thrombus Complement C5a Gradient
During mechanical thrombectomy, before recanalization
Trans-Thrombus Malondialdehyde Gradient
During mechanical thrombectomy, before recanalization
- +7 more secondary outcomes
Other Outcomes (6)
Symptomatic intracranial hemorrhage
24 (±12) hours
Any intracranial hemorrhage
24 (±12) hours
Extracranial bleeding
24 (±12) hours
- +3 more other outcomes
Study Arms (1)
Prospective Mechanical Thrombectomy Cohort
Adults with acute ischemic stroke due to anterior circulation large vessel occlusion who undergo clinically indicated mechanical thrombectomy. All participants receive standard stroke care determined by the treating clinical team; no experimental intervention is assigned. Paired arterial blood samples are collected during thrombectomy from sites proximal and distal to the thrombus. A peripheral venous blood sample collected at hospital admission is used as a supportive systemic reference. Clinical, imaging, procedural, and 90-day functional outcome data are collected prospectively.
Interventions
Adults with acute ischemic stroke due to anterior circulation large vessel occlusion who undergo clinically indicated mechanical thrombectomy. All participants receive standard stroke care determined by the treating clinical team; no experimental intervention is assigned. Paired arterial blood samples are collected during thrombectomy from sites proximal and distal to the thrombus. A peripheral venous blood sample collected at hospital admission is used as a supportive systemic reference. Clinical, imaging, procedural, and 90-day functional outcome data are collected prospectively.
Eligibility Criteria
This single-center prospective observational cohort will enroll consecutive adults with acute ischemic stroke due to anterior circulation large vessel occlusion who undergo clinically indicated mechanical thrombectomy. Participants receive standard stroke care determined by the treating clinical team; no experimental treatment is assigned. During thrombectomy, paired arterial plasma samples are collected from locations proximal and distal to the thrombus when technically feasible and without delaying or altering routine treatment. An admission peripheral venous blood sample is collected as a supportive reference for systemic inflammation. Clinical, imaging, procedural, laboratory, and 90-day follow-up data are collected prospectively.
You may qualify if:
- Age 18 years or older.
- Acute ischemic stroke caused by anterior circulation large vessel occlusion, confirmed by routine vascular imaging or digital subtraction angiography.
- Undergoing clinically indicated mechanical thrombectomy according to routine clinical practice.
- Provision of written informed consent by the participant or legally authorized representative, in accordance with local ethics requirements.
You may not qualify if:
- Posterior circulation large vessel occlusion.
- Mechanical thrombectomy not performed.
- Known active systemic infection, active malignancy, or chronic inflammatory/autoimmune disease requiring systemic immunosuppressive treatment, when these conditions are expected to substantially affect inflammatory biomarker measurements.
- Pregnancy or breastfeeding, if required by the local ethics committee.
- Enrollment in another interventional study that could affect inflammatory biomarker measurements or clinical outcome assessment.
- Inability to obtain informed consent, where consent from a legally authorized representative is not permitted or cannot be obtained.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Zhongshan Hospital Xiamen University
Xiamen, Fujian, 361004, China
Related Publications (23)
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PMID: 31248666BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Xingyu Chen, MD
Zhongshan Hospital Xiamen University
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Chief Physician, Department of Neurology
Study Record Dates
First Submitted
August 4, 2026
First Posted
August 10, 2026
Study Start
August 1, 2026
Primary Completion (Estimated)
August 1, 2028
Study Completion (Estimated)
August 1, 2029
Last Updated
August 10, 2026
Record last verified: 2026-08
Data Sharing
- IPD Sharing
- Will not share
Individual participant data, including clinical and biospecimen data, will not be publicly shared because of ethical, privacy, informed-consent, and institutional restrictions. Requests for access to de-identified data for scientifically valid purposes may be considered by the principal investigator and the institution, subject to applicable ethics approval and a data-use agreement. Contact: Xingyu Chen, 2005chenxingyu@163.com