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NCT Number: NCT06388148

Endovascular Treatment for eXtra-Large Ischemic Stroke

The role of endovascular thrombectomy in patients with extra-large ischemic burden is still unclear. The XL STROKE-2 randomized trial is aiming to investigate the efficacy and safety of mechanical thrombectomy in acute extra-large ischemic stroke patients with large vessel occlusion.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

The First Affiliated Hospital, Hengyang Medical School, University of South China, Hengyang, Hunan, China

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About this study

Several randomized trials have shown that endovascular thrombectomy improve functional outcomes in acute ischemic stroke patients with large vessel occlusion. Recently, six randomized controlled trials demonstrated the efficacy and safety of endovascular thrombectomy for large infarct patients (defined as Alberta Stroke Program Early Computed Tomography Score [ASPECTS] ≥3 or infarct core <100ml). Patients with extra-large infarct core (volume greater than 100 mL, ASPECTS score of 0 to 2) accounted for a small proportion of these trials. Therefore, the role of endovascular thrombectomy in patients with extra-large ischemic burden is still unclear. That is to say, exactly where the lower limit of endovascular thrombectomy is unknown. The XL STROKE-2 randomized trial is aiming to investigate the efficacy and safety of mechanical thrombectomy in acute extra-large ischemic stroke patients with large vessel occlusion.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age 18 years or older, and modified Rankin scale score = 0 or 1 in patients 80 years or older;
  • Acute ischemic stroke within 6 hours from last known well to randomization, or with negative MRI-FLAIR (no change on FLAIR sequence and presence of infarct on MRI-DWI) if > 6 hours or unknown last known well time;
  • Occlusion of the internal carotid artery, M1 or M2 segment of the middle cerebral artery confirmed by CTA/MRA/DSA;
  • Baseline ASPECTS score of 0-2 or infarct core volume ≥100ml;
  • The patient or patient's representative signs a written informed consent form.

Exclusion criteria

  • CT or MR evidence of hemorrhage;
  • Evidence of mass effect with ventricular effacement, midline shift or herniation on baseline imaging;
  • Vessel tortuosity where it is expected that the thrombectomy device will not be able to reach the occlusion site or result in unstable access;
  • History of bleeding disorders, severe heart, liver or kidney disease, or sepsis;
  • Currently participating in another investigational drug study;
  • Any terminal illness with life expectancy less than 6 months.

Treatment and study plan

Medical Management

Drug

Medical management includes IV thrombolysis, antiplatelet, and/or anticoagulation.

Endovascular Thrombectomy

Procedure

Endovascular thrombectomy with stent-retriever, local aspiration, angioplasty, and/or stenting.

Primary outcomes

  1. Modified Rankin Scale score

    Time frame: 90 days after randomization

    Modified Rankin scale score (mRS): scores range from 0 to 6, with 0 indicating no disability, 1 no clinically significant disability, 2 slight disability, 3 moderate disability but able to walk unassisted, 4 moderately severe disability, 5 severe disability, and 6 death

Secondary outcomes

  1. Rate of successful reperfusion

    Time frame: Within 5 minutes at the end of angiogram

    Final reperfusion grade of 2b-3 on eTICI scale (This 7-point compilation of TICI grades, termed the expanded TICI (eTICI), reflects all previously reported thresholds used to define reperfusion after endovascular stroke therapy. In brief, eTICI grade 0 is equivalent to no reperfusion or 0% filling of the downstream territory; eTICI 1 reflects thrombus reduction without any reperfusion of distal arteries; eTICI 2a is reperfusion in less than half or 1-49% of the territory; eTICI 2b50 is 50-66% reperfusion, exceeding the modified TICI (mTICI) 2B threshold but below the original TICI 2B cut-off point; eTICI 2b67 is 67-89% reperfusion, exceeding TICI but below TICI 2C; eTICI 2c is equivalent to TICI 2C or 90-99% reperfusion; and eTICI 3 is complete or 100% reperfusion, tantamount to TICI 3.)

  2. Rate of excellent outcome

    Time frame: 90 days after randomization

    Score of 0-1 on the modified Rankin scale

  3. Rate of functional independence

    Time frame: 90 days after randomization

    Score of 0-2 on the modified Rankin scale

  4. Rate of independent ambulation

    Time frame: 90 days after randomization

    Score of 0-3 on the modified Rankin scale

Study contacts

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

Zhongfan Ruan

CONTACT

[email protected]

15616320002

Zhongming Qiu

CONTACT

[email protected]

13236599269

Sponsors and collaborators

Lead sponsor

Zhongming Qiu

Other

Collaborators

  • Affiliated Hangzhou First People's Hospital, School of Medicine, Westlake University
  • Longyan First Affiliated Hospital of Fujian Medical University
  • Taizhou First People's Hospital
  • The First Affiliated Hospital of University of South China
  • Xiangtan Central Hospital
  • Zhangzhou Affiliated Hospital of Fujian Medical University

Registry information

Official study title

Efficacy and Safety of Endovascular Thrombectomy Plus Medical Management Versus Medical Management Alone in Acute Ischemic Stroke Patients With Large Vessel Occlusion and Extra-Large Infarct Core: A Multicenter, Randomized Controlled Trial

Acronym: XL STROKE-2

Important dates

Study start
2024
Primary completion
2026
Study completion
2027
First posted
Apr 29, 2024
Registry last updated
Dec 26, 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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