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The Endovascular Stroke thrombectomy for Patients with active Oncologic Illness aiming at Recovery registry

The Endovascular Stroke thrombectomy for Patients with active Oncologic Illness aiming at Recovery registry - ESPOIR registry

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000057739
Enrollment
300
Registered
2025-05-01
Start date
2025-04-26
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Acute ischemic stroke due to large vessel occlusion associated with active malignancy

Interventions

None listed

Sponsors

University of Tsukuba
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Adults aged 18 years or older. (2) Patients who were hospitalized and treated at participating institutions between January 1, 2018, and December 31, 2024. (3) Patients with acute ischemic stroke who were admitted within 24 hours from symptom onset or from last known well time, who also had active malignancy (including in-hospital stroke onset and patients diagnosed with active malignancy after stroke onset). (4) Patients who developed ischemic stroke due to acute large vessel occlusion (common carotid artery [CCA], internal carotid artery [ICA], M1 or M2 segment of the middle cerebral artery [MCA], vertebral artery [VA], or basilar artery [BA]). (5) Patients with a National Institutes of Health Stroke Scale (NIHSS) score of 6 or higher at onset. (6) Patients with an Alberta Stroke Program Early CT Score (ASPECTS) of 3 or higher for anterior circulation occlusions, or a posterior circulation Acute Stroke Prognosis Early CT Score (pc-ASPECTS) of 6 or higher for posterior circulation occlusions, assessed by non-contrast CT or diffusion-weighted MRI (DWI).

Exclusion criteria

Exclusion criteria: (1) The patient or the legal representative expresses a refusal to participate. (2) The attending physician determines that the patient is ineligible for enrollment in the study.

Design outcomes

Primary

MeasureTime frame
Primary Efficacy Endpoint: A composite outcome of either discharge to home within 90 days after stroke onset, or a mRS score of 0-2 or a return to the pre-stroke mRS score at 90 days after onset. Primary Safety Endpoints: All-cause mortality within 90 days after stroke onset, symptomatic intracranial hemorrhage (sICH) within 7 days after onset.

Secondary

MeasureTime frame
Discharge to home within 90 days after onset. At discharge and at 90 days after onset: mRS score, mRS 0-2, return to the pre-stroke mRS score, composite outcome of achieving mRS 0-2 or returning to the pre-stroke mRS score. Initiation or resumption of active cancer treatment (surgical resection, chemotherapy, radiotherapy, or other therapies aimed at cure or life-prolongation) within 90 days after stroke onset. Asymptomatic intracranial hemorrhage (ICH) or any ICH (classified according to the Heidelberg Bleeding Classification) within 7 days after onset. Rate of successful reperfusion (defined as modified Thrombolysis in Cerebral Infarction [mTICI] grade 2b, 2c, or 3) and rate of complete reperfusion in the EVT group. Subgroup analyses stratified by clinically relevant factors such as stroke subtype, cancer stage and others.

Countries

Japan

Contacts

Public ContactMIKITO HAYAKAWA

University of Tsukuba Hospital Department of Stroke and Cerebrovascular Diseases

mikito-h@jc4.so-net.ne.jp0298533220

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026