NCT07754942

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

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
50

participants targeted

Target at P25-P50 for all trials

Timeline
37mo left

Started Aug 2026

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress1%
Aug 2026Aug 2029

Study Start

First participant enrolled

August 1, 2026

Completed
3 days until next milestone

First Submitted

Initial submission to the registry

August 4, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

August 10, 2026

Completed
2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2028

Expected
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2029

Last Updated

August 10, 2026

Status Verified

August 1, 2026

Enrollment Period

2 years

First QC Date

August 4, 2026

Last Update Submit

August 4, 2026

Conditions

Keywords

Mechanical ThrombectomyAnterior Circulation Large Vessel OcclusionTrans-Thrombus GradientInflammatory BiomarkersReperfusion InjuryModified Rankin ScaleInterleukin-6

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.

Other: Prospective Mechanical Thrombectomy Cohort

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.

Prospective Mechanical Thrombectomy Cohort

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

Location

Related Publications (23)

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  • Goyal M, Menon BK, van Zwam WH, Dippel DW, Mitchell PJ, Demchuk AM, Davalos A, Majoie CB, van der Lugt A, de Miquel MA, Donnan GA, Roos YB, Bonafe A, Jahan R, Diener HC, van den Berg LA, Levy EI, Berkhemer OA, Pereira VM, Rempel J, Millan M, Davis SM, Roy D, Thornton J, Roman LS, Ribo M, Beumer D, Stouch B, Brown S, Campbell BC, van Oostenbrugge RJ, Saver JL, Hill MD, Jovin TG; HERMES collaborators. Endovascular thrombectomy after large-vessel ischaemic stroke: a meta-analysis of individual patient data from five randomised trials. Lancet. 2016 Apr 23;387(10029):1723-31. doi: 10.1016/S0140-6736(16)00163-X. Epub 2016 Feb 18.

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    PMID: 25882510BACKGROUND
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MeSH Terms

Conditions

Ischemic StrokeReperfusion Injury

Condition Hierarchy (Ancestors)

StrokeCerebrovascular DisordersBrain DiseasesCentral Nervous System DiseasesNervous System DiseasesVascular DiseasesCardiovascular DiseasesPostoperative ComplicationsPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • Xingyu Chen, MD

    Zhongshan Hospital Xiamen University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Yibin Xiao, MD

CONTACT

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

Locations