Predictors of Good Outcomes of Thrombectomy In Large Infarct Core Stroke

Sponsor
115 People's Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT06016348
Collaborator
University of Medicine and Pharmacy at Ho Chi Minh City (Other)
160
4
28.2
40
1.4

Study Details

Study Description

Brief Summary

Identify the factors associated with a favorable clinical outcome in participants with acute ischemic stroke and large core infarcts within 24 hours of onset who are treated with endovascular intervention.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Endovascular treatment

Detailed Description

In 2022 and early 2023, three randomized controlled trials-RESCUE-JAPAN LIMIT, SELECT 2, and ANGEL ASPECT-were published in the New England Journal of Medicine. These trials demonstrated the effectiveness and safety of endovascular intervention using clot retrieval devices in participants with acute ischemic stroke and large core infarcts. However, the rate of participants achieving a good recovery remains low, while the mortality and disability rates are very high.

Moreover, in Vietnam, the acute stroke treatment process has not been optimized, and the facilities and equipment for monitoring neurointensive care are not fully equipped. As a result, endovascular intervention using clot retrieval devices in participants with large core infarcts has not been widely implemented in the investigator's country, and the effectiveness and safety of this treatment method have not been clearly evaluated.

Addressing this issue is crucial for improving the quality of life and reducing the mortality and disability rates caused by stroke in this participant group. This study aims to provide new insights into the use of endovascular intervention for treating acute ischemic stroke with a large core infarct volume, thereby supporting clinical decision-making and improving treatment outcomes for participants with acute ischemic stroke and large core infarcts.

Study Design

Study Type:
Observational [Patient Registry]
Anticipated Enrollment :
160 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Predictors of Good Outcomes of Thrombectomy In Stroke Patients Within 24 Hours From Symptom Onset With Large Infarct Core
Actual Study Start Date :
Jul 28, 2023
Anticipated Primary Completion Date :
Sep 1, 2025
Anticipated Study Completion Date :
Dec 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Good outcome

mRS of 0-3; mRS of 0-2

Procedure: Endovascular treatment
This procedure is instrumental in restoring cerebral blood flow by addressing the clot-induced obstruction within brain-supplying blood vessels.
Other Names:
  • Mechanical thrombectomy
  • Unfavorable outcomes

    mRS of 4-6

    Procedure: Endovascular treatment
    This procedure is instrumental in restoring cerebral blood flow by addressing the clot-induced obstruction within brain-supplying blood vessels.
    Other Names:
  • Mechanical thrombectomy
  • Outcome Measures

    Primary Outcome Measures

    1. The Modified Rankin Scale (mRS) of 0-3 [90 (± 14 days) after procedure]

      The rate of independent ambulation (mRS 0-3). The scale runs from 0-6, running from perfect health without symptoms to death.

    Secondary Outcome Measures

    1. mRS of 0-2 [90 (± 14 days) after procedure]

      The rate of functional independence (mRS 0-2)

    2. mRS of 0-5 [90 (± 14 days) after procedure]

      The survival rate

    3. Symptomatic intracerebral hemorrhage (sICH) [72 hours]

      sICH means any hemorrhage with neurological deterioration, as indicated by an NIHSS score that was higher by ≥4 points than the value at baseline or the lowest value in the first 72 hours or any hemorrhage leading to death.

    4. Early neurological deterioration [72 hours]

      Clinical worsening that was higher by ≥4 points than the value at baseline during the first 72 h after ischaemic stroke.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Age ≥ 18-year-old

    • Patients presenting with acute ischaemic stroke within 24 hours of stroke onset

    • Received mechanical thrombectomy within 24 hours of stroke onset

    • Imaging criteria include:

    • Large vessel occlusion on CT Angiography or MR Angiography (MRA) including tandem occlusion of the internal carotid artery and middle cerebral artery or internal carotid artery.

    • Core infarct criteria:

    1. ASPECTS ≤5 on non-contrast CT or diffusion-weighted imaging (DWI).

    2. ASPECTS score >5 and core infarct volume of 50-150 ml on CT perfusion (CTP) or reduced cerebral blood flow (rCBF) <30% on CTP or apparent diffusion coefficient (ADC) <620 × 10-6 mm2/s on DWI.

    Exclusion Criteria:
    • Patients presenting with acute ischaemic stroke >24 hours of stroke onset

    • Intracranial hemorrhage identified by CT or MRI

    • Pre-stroke modified Rankin Score (mRS) score of >2 (indicating previous disability)

    • Any terminal illness such that the patient has a life expectancy of less than 1 year.

    • Patients with active cancer and undergoing treatment for cancer are excluded,

    • Pregnancy

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Can Tho Central General Hospital Cần Thơ Vietnam
    2 Da Nang Stroke Center Da Nang Vietnam
    3 115 PEOPLE's HOSPITAL Ho Chi Minh City Vietnam 70000
    4 University Medical Center Ho Chi Minh City Vietnam 70000

    Sponsors and Collaborators

    • 115 People's Hospital
    • University of Medicine and Pharmacy at Ho Chi Minh City

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Trung Nguyen, Principal Investigator, 115 People's Hospital
    ClinicalTrials.gov Identifier:
    NCT06016348
    Other Study ID Numbers:
    • 115
    First Posted:
    Aug 29, 2023
    Last Update Posted:
    Aug 29, 2023
    Last Verified:
    Aug 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Trung Nguyen, Principal Investigator, 115 People's Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 29, 2023