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Efficacy and Safety of Bailout Intracranial Angioplasty or Stenting After Thrombectomy for Acute Intracranial Atherosclerotic Large Vessel Occlusion (ANGEL-REBOOT 2)

25. mai 2026 oppdatert av: Feng Gao

Efficacy and Safety of Bailout Intracranial Angioplasty or Stenting After Thrombectomy for Acute Intracranial Atherosclerotic Large Vessel Occlusion: A Clinical Trial Combining a Randomized Controlled Trial and a Concurrent Prospective Observational Cohort

A multicenter, randomized, open-label, blinded-endpoint trial with a concurrent prospective observational cohort to compare bailout intracranial angioplasty or stenting versus standard therapy on functional outcome, stroke recurrence, and mortality in patients with acute intracranial atherosclerotic stenosis-related large vessel occlusion after thrombectomy.

Studieoversikt

Detaljert beskrivelse

This is a clinical trial with a composite design, consisting of: (1) a multicenter, prospective, open-label, blinded-endpoint randomized controlled trial (RCT) for patients with successful recanalization but residual severe stenosis (>70%) after thrombectomy, and (2) a concurrent prospective observational cohort for patients with failed recanalization. Patients with acute ischemic stroke due to intracranial atherosclerotic stenosis-related large vessel occlusion (ICAS-LVO) within 24 hours of symptom onset who undergo up to two thrombectomy passes are assessed. Those achieving successful recanalization (expanded Thrombolysis in Cerebral Infarction [eTICI] grade ≥2b) but with residual stenosis ≥70% are enrolled in the RCT and randomly assigned in a 1:1 ratio to receive either bailout angioplasty or stenting (BAOS) (intervention group) or standard therapy (control group). Randomization is performed using a centralized interactive web response system with a minimization method, stratified by baseline National Institutes of Health Stroke Scale score (6-15 vs. ≥16), time from symptom onset to puncture (≤6 hours vs. 6-24 hours), and occlusion site (anterior circulation vs. posterior circulation). For patients who fail to achieve successful recanalization (eTICI 0-2a) after at least two thrombectomy passes, they are enrolled in the concurrent prospective observational cohort without randomization, and subsequent treatment (including continued thrombectomy, BAOS, or termination of the procedure) is at the discretion of the treating physician. The primary endpoint is the modified Rankin Scale (mRS) score at 90 days (±7 days) after randomization or enrollment. Key secondary efficacy endpoints include the proportion of patients with mRS scores of 0-1, 0-2, and 0-3 at 90 days; stroke recurrence in the target vessel territory within 90 days and 1 year; NIHSS score at 24 hours; and quality of life measures at 90 days and 1 year. Safety endpoints include symptomatic intracranial hemorrhage within 24 hours (defined by the Heidelberg Bleeding Classification), any intracranial hemorrhage within 24 hours, mortality at 7 days, 90 days, and 1 year, and procedure-related complications (e.g., arterial perforation, dissection, or distal embolization). Follow-up assessments are performed at 24 hours, 7 days or discharge (whichever occurs first), 90 days, and every 3 months thereafter until 1 year after randomization or enrollment.

Studietype

Intervensjonell

Registrering (Antatt)

420

Fase

  • Ikke aktuelt

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studiesteder

    • Beijing Municipality
      • Beijing, Beijing Municipality, Kina, 100070
        • Beijing Tiantan Hospital, Capital Medical University

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Nei

Beskrivelse

Inclusion Criteria:

  1. Age≥18 years.
  2. Time interval from symptom onset to puncture ≤24 hours.
  3. National Institute of Health Stroke Scale (NIHSS) Score ≥6 before randomisation.
  4. Pre-stroke modified Rankin Scale (mRS) of 0-2.
  5. Each patient or their legal representative must provide written informed consent before enrolment.

Imaging Inclusion Criteria:

  1. For patients with anterior circulation stroke, a CT or DWI-based Alberta Stroke Program Early CT Score (ASPECTS) of ≥6 is required.
  2. For patients with posterior circulation stroke, CT or DWI-based posterior circulation ASPECTS (pc-ASPECTS) of ≥6 and Pons-Midbrain Index (PMI) of <3 are required.

Angiographic Inclusion Criteria:

  1. Acute ischemic stroke (AIS) resulting from large vessel occlusion (LVO) involving the intracranial internal carotid artery, the M1 segment of the middle cerebral artery, the V4 segment of the vertebral artery, or the basilar artery, with high suspicion of intracranial atherosclerotic stenosis-related large-vessel occlusion (ICAS-LVO).
  2. Part 1 (RCT): Successful recanalization of the occluded artery (eTICI ≥ 2b) with residual stenosis ≥ 70% after 1-2 thrombectomy attempts.

    Part 2 (Prospective observational cohort): Failure to achieve successful recanalization (eTICI 0-2a) after at least two thrombectomy attempts. All other inclusion criteria are identical to those for Part 1.

  3. Occluded artery amenable to angioplasty (balloon dilation and/or stenting) by the judgement of the treating neurointerventionalist.

Exclusion Criteria:

  1. Any sign of intracranial hemorrhage (ICH, except microbleeds) on baseline brain imaging.
  2. CT or MR imaging evidence of intracranial tumor (except small meningiomas or cerebral aneurysms < 3mm in diameter).
  3. Any indication of intracranial vessel perforation during thrombectomy..
  4. Presence of tandem lesion in the extracranial segment of the internal carotid artery or vertebral artery, or intracranial arterial stenosis with distal vessel occlusion..
  5. Stenosis caused by non-atherosclerotic intracranial arteriopathies (e.g., autoimmune vasculitis, vasospasm, cerebral artery dissection).
  6. Evidence of cardioembolism (e.g., atrial fibrillation, prosthetic heart valve, infective endocarditis, mitral stenosis, atrial myxoma, intracardiac thrombus/vegetation, left ventricular aneurysm, etc.).
  7. Contraindication for antiplatelet treatment.
  8. Excessive vascular tortuosity or anatomical variants that may preclude successful delivery or positioning of interventional devices.
  9. History of contraindication to the use of contrast medium.
  10. Refractory hypertension (defined as systolic blood pressure>185 mmHg or diastolic blood pressure>110 mmHg) that cannot be controlled by drug treatment.
  11. Known hereditary or acquired bleeding tendency, lack of coagulation factors, or oral anticoagulants with INR>1.5.
  12. Blood glucose<2.8 or>22.2 mmol/L; Platelet count<100*109/L, serum creatinine>2.0 g/L (177 μ mol/L), or glomerular filtration rate<30 ml/(min*1.73 m2).
  13. Concurrent participation in another drug or device trial, or expected participation within the following 3 months.
  14. Patients whose life expectancy is less than 1 year (such as patients with malignant tumor, advanced cardiopulmonary disease, etc.).
  15. Known pregnancy or lactation, or positive pregnancy test before randomization (or before enrollment).
  16. Known dementia or psychiatric disorder that precludes completion of neurological assessments and follow-up.
  17. Any other condition deemed by the site investigator to make the patient unsuitable for participation.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Enkelt

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Intervention group
Bailout Angioplasty or Stenting (BAOS) Group
Balloon angioplasty and/or stent placement for residual severe stenosis (≥70%) after successful thrombectomy; combined with medical management (intravenous tirofiban, followed by dual antiplatelet therapy with aspirin 100 mg/day and clopidogrel 75 mg/day for 90 days, then single antiplatelet therapy thereafter; and cerebrovascular risk factor management).
Annen: Control group
Standard Ttherapy Group
Endovascular thrombectomy performed according to guideline recommendations, without additional endovascular intervention; combined with medical management (intravenous tirofiban as needed, dual antiplatelet therapy with aspirin 100 mg/day and clopidogrel 75 mg/day for 90 days, then single antiplatelet therapy thereafter; and cerebrovascular risk factor management).

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
The primary endpoint is the mRS score at 90 (±7) days after randomization (or after enrollment), analyzed as an ordinal variable
Tidsramme: 90±7 days after randomization (or after enrollment)
The modified Rankin scale (mRS) ranged from 0 to 6, with a score of 0 indicating no disability, 1 no clinically significant disability, 2 slight disability, 3 moderate disability but remaining able to walk unassisted, 4 moderately severe disability,5 severe disability, and 6 death.
90±7 days after randomization (or after enrollment)

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
The proportion of mRS 0-1, 0-2 and 0-3 at 90 (±7) days
Tidsramme: 90±7 days after randomization (or after enrollment)
The proportion of mRS 0-1, 0-2 and 0-3 at 90 (±7) days.
90±7 days after randomization (or after enrollment)
The rate of stroke recurrence in the target vessel territory within 90 (±7) days
Tidsramme: 90±7 days after randomization (or after enrollment)
Stroke recurrence in the target vessel territory within 90 (±7) days.
90±7 days after randomization (or after enrollment)
NIHSS score at 24 (±6/+12) hours
Tidsramme: 24 (-6/+12) hours after randomization (or after enrollment)
The National Institute of Health Stroke Scale (NIHSS) ranged from 0 to 42, with higher scores indicating greater neurologic deficits.
24 (-6/+12) hours after randomization (or after enrollment)
European Five Dimensional Health Scale Level 5 (EQ-5D-5L) score at 90±7 days
Tidsramme: 90±7 days after randomization (or after enrollment)
EuroQol Five Dimensions (EQ-5D-5L) is a standardized instrument for measuring the general health status. Rated level can be coded as a number 1, 2, 3, 4 or 5, which indicates having no problems for 1, having some problems for 2, having moderate problems for 3, having serious problems for 4 and having extreme problems for 5.
90±7 days after randomization (or after enrollment)
Patency of the target vessel at 24 (±6/+12) hours after the procedure, as confirmed by CTA, MRA, DSA, or TCD
Tidsramme: 24 (-6/+12) hours after randomization (or after enrollment)
Patency of the target vessel at 24 (±6/+12) hours after the procedure, as confirmed by CTA, MRA, DSA, or TCD.
24 (-6/+12) hours after randomization (or after enrollment)
The mRS score at 1 year (±30 days), analyzed as an ordinal variable
Tidsramme: 1 year (±30 days) after randomization (or after enrollment)
The modified Rankin scale (mRS) ranged from 0 to 6, with a score of 0 indicating no disability, 1 no clinically significant disability, 2 slight disability, 3 moderate disability but remaining able to walk unassisted, 4 moderately severe disability,5 severe disability, and 6 death.
1 year (±30 days) after randomization (or after enrollment)
The proportion of mRS 0-1, 0-2 and 0-3 scores at 1 year (± 30 days)
Tidsramme: 1 year (±30 days) after randomization (or after enrollment)
The proportion of mRS 0-1, 0-2 and 0-3 scores at 1 year (± 30 days).
1 year (±30 days) after randomization (or after enrollment)
The rate of stroke recurrence in the target vessel territory within 1 year (± 30 days)
Tidsramme: 1 year (±30 days) after randomization (or after enrollment)
Stroke recurrence in the target vessel territory within 1 year (± 30 days).
1 year (±30 days) after randomization (or after enrollment)
Patency of the target vessel at 1 year (± 30 days) after the procedure, as confirmed by CTA, MRA, DSA, or TCD
Tidsramme: 1 year (±30 days) after randomization (or after enrollment)
Patency of the target vessel at 1 year (± 30 days) after the procedure, as confirmed by CTA, MRA, DSA, or TCD.
1 year (±30 days) after randomization (or after enrollment)
European Five Dimensional Health Scale Level 5 (EQ-5D-5L) score at 1 year (±30 days)
Tidsramme: 1 year (±30 days) after randomization (or after enrollment)
EuroQol Five Dimensions (EQ-5D-5L) is a standardized instrument for measuring the general health status. Rated level can be coded as a number 1, 2, 3, 4 or 5, which indicates having no problems for 1, having some problems for 2, having moderate problems for 3, having serious problems for 4 and having extreme problems for 5.
1 year (±30 days) after randomization (or after enrollment)

Andre resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
The rate of any Symptomatic intracranial hemorrhage (sICH) defined as the Heidelberg classification within 24 hours
Tidsramme: 24 (-6/+12) hours after randomization (or after enrollment)
Heidelberg standard was defined as new intracranial hemorrhage detected by brain imaging associated with any of the item below: 4 points total NIHSS at the time of diagnosis compared to immediately before worsening. 2 point in one NIHSS category. Leading to intubation/hemicraniectomy/ventricular drainage placement or other major medical/surgical intervention. Absence of alternative explanation for deterioration.
24 (-6/+12) hours after randomization (or after enrollment)
The rate of all-cause mortality within 90 days
Tidsramme: 90±7 days after randomization (or after enrollment)
All cause of mortality within 90 days.
90±7 days after randomization (or after enrollment)
The rate of any intracranial hemorrhage identified by CT or MRI imaging within 24 hours after randomization
Tidsramme: 24 (-6/+12) hours after randomization
Any intracranial hemorrhage identified by CT or MRI imaging within 24 (-6/+12) hours after randomization.
24 (-6/+12) hours after randomization
Procedure-related complications, including arterial perforation, arterial dissection, and embolization to a new vascular territory
Tidsramme: At the end of the procedure or intraoperatively
Procedure-related complications, including arterial perforation, arterial dissection, and embolization to a new vascular territory.
At the end of the procedure or intraoperatively
Procedure-related complications: arterial perforation, arterial dissection, and new territorial embolism, etc
Tidsramme: At the end of the procedure or intraprocedurally
Procedure-related complications: arterial perforation, arterial dissection, and new territorial embolism, etc.
At the end of the procedure or intraprocedurally
The rate of all-cause mortality within 1 year (± 30 days)
Tidsramme: 1 year (±30 days) after randomization (or after enrollment)
The rate of all-cause mortality within 1 year (±30 days).
1 year (±30 days) after randomization (or after enrollment)
The rate of any Symptomatic intracranial hemorrhage (sICH) defined as the Heidelberg classification or any intracranial hemorrhage within 1 year (±30 days)
Tidsramme: 1 year (±30 days) after randomization (±30 days)
Any Symptomatic intracranial hemorrhage (sICH) defined as the Heidelberg classification or any intracranial hemorrhage within 1 year (±30 days).
1 year (±30 days) after randomization (±30 days)

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Sponsor

Etterforskere

  • Hovedetterforsker: Feng Gao, MD, Beijing Tiantan Hospital

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

1. juni 2026

Primær fullføring (Antatt)

1. juni 2027

Studiet fullført (Antatt)

1. juni 2028

Datoer for studieregistrering

Først innsendt

25. mai 2026

Først innsendt som oppfylte QC-kriteriene

25. mai 2026

Først lagt ut (Faktiske)

1. juni 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

1. juni 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

25. mai 2026

Sist bekreftet

1. mai 2026

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

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NEI

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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