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REperfusion Therapy for Acute Ischemic STrOke Due to Large aRtEry Occlusion

REperfusion Therapy for Acute Ischemic STrOke Due to Large aRtEry Occlusion

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05311605
Acronym
RESTORE
Enrollment
1600
Registered
2022-04-05
Start date
2023-02-23
Completion date
2024-12-31
Last updated
2024-03-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Endovascular Treatment, Mechanical Thrombectomy, Perfusion Imaging, Stroke, Vascular Occlusion

Keywords

ischemic stroke, vascular occlusion, endovascular treatment, mechanical thrombectomy, perfusion imaging

Brief summary

The aim of the study was to establish a clinical and advanced imaging database of acute ischemic stroke patients treated with mechanical thrombectomy due to large vessel occlusion of anterior circulation within 24 hours from stroke onset in China, and to investigate the predictors and potential mechanisms of futile recanalization after mechanical thrombectomy.

Detailed description

The time-window of mechanical thrombectomy for ischemic stroke has extended from 4.5 hours to 24 hours based on the results of the DAWN and DEFUSE 3 trials. However, evidence on the effectiveness and safety of mechanical thrombectomy within 24 hours in the real-world is insufficient. This is a multi-center, prospective, registry cohort study that acute ischemic stroke patients treated with mechanical thrombectomy due to large vessel occlusion of anterior circulation within 24 hours from stroke onset in China. A retrospective dataset was also build in these stroke centers for analysis. A total of 1600 patients with advanced imaging data were anticipated to be enrolled.

Interventions

None listed

Sponsors

National Natural Science Foundation of China
CollaboratorOTHER_GOV
Beijing Municipal Science & Technology Commission
CollaboratorOTHER
Beijing Municipal Administration of Hospitals
CollaboratorOTHER_GOV
Beijing Tiantan Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* Older than 18 years; * Perfusion imaging completed including CTA+CTP or MRA+PWI+DWI before thrombectomy * Large vessel occlusion of cerebral anterior circulation (ICA, MCA-M1 or MCA-M2) confirmed by CTA or MRA, planned to receive or received stenting or aspiration thrombectomy * Time intervals ≤ 24 hours from stroke onset to groin puncture.(fulfilled the inclusion of DAWN or DEFUSE 3 trial if the time intervals from stroke onset to groin puncture was ≥6 hours) * mRS score ≤2 before admission * Informed consent obtained for longitudinal enrolled patients, waived of consent for retrospectively included cases

Exclusion criteria

* Had a history of infective disease, immunity disease, radiotherapy at head or neck, carotid dissection or other carotid disease. * Unable to receive CT or MR scan due to heart failure, cardiac pacemaker, metal implants or claustrophobia, etc. * Unable to be injected with contrast agent due to allergy, renal dysfunction, etc. * Unlikely to adhere to the study protocol or follow-up ( life expectancy ≤ 3 months) * Already participated in other drug trials

Design outcomes

Primary

MeasureTime frameDescription
Favorable functional outcome3 months from stroke onsetproportion of mRS score 0-2 at 3 months. The modified Rankin Scale (mRS) has a minimum value of 0 and maximum value of 6. Higher value indicated worse functional outcome

Secondary

MeasureTime frameDescription
EQ-5D score at at 90 days3 months from stroke onsetEQ-5D score at 3 months. EuroQol Five Dimensions Questionnaire scale (EQ-5D score) has a minimum value of 0 and maximum value of 100. Lower value indicated worse functional outcome
Neurological improvement at 24 hours24 hours from stroke onsetNIHSS score \<=1 or improvement of NIHSS score\>=4 compared with baseline NIHSS. National Institution Health Stroke Scale (NIHSS) has a minimum value of 0 and maximum value of 45. Higher value indicated worse severity of neurological impairment.
recanalization post-operation(Day 0) immediately the surgeon thought the thrombectomy completed and performed a second cerebral angiography .proportion of eTICI 2b50/2c/3. Thrombectomy is a surgical operation using a retrieve stent or aspiration catheter to remove the thrombus inside an occluded vessel and achieve recanalization.The eTICI is a scale to assess the degree of recanalization. So, once the surgeon thought he completed the thrombectomy, he needed to perform a cerebral angiography to assess the degree of recanalization using eTICI.
recanalization at 24 hours24 hours after thrombectomy completedproportion of eTICI 2b50/2c/3
Ordinal distribution of mRS at 90 days3 months from stroke onsetNumber of participants with the ordinal distribution of mRS at 90 days
Excellent functional outcome at 90 days3 months from stroke onsetproportion of mRS score 0-1 at 3 months

Other

MeasureTime frameDescription
Mortality at 90 days90 days after thrombectomy completedMortality of all-cause
Infarction volume at 24 hours24 hours after thrombectomy completedinfarction volume: volume of the tissue with CBF \<30% or ADC\<600×10-6mm2/s
symptomatic intracerebral hemorrhage at 36 hours36 hours after thrombectomy completedsymptomatic intracerebral hemorrhage based on Heidelberg criterion

Countries

China

Contacts

Primary ContactYunyun Xiong, MD, PhD
xiongyunyun@bjtth.org00861059975213

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026