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Exploratory Research on Safety and Efficacy of Adjunctive Intra-arterial adenosine following Successful Endovascular Thrombectomy in Patients with Posterior Circulation Large Vessel Occlusion Acute Ischemic Stroke

Exploratory Research on Safety and Efficacy of Adjunctive Intra-arterial adenosine following Successful Endovascular Thrombectomy in Patients with Posterior Circulation Large Vessel Occlusion Acute Ischemic Stroke

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500096821
Enrollment
Unknown
Registered
2025-02-07
Start date
2025-02-07
Completion date
Unknown
Last updated
2025-02-10

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

Conditions

acute ischemic stroke

Interventions

Experimental group:Adjunctive Intra-arterial adenosine following successful endovascular thrombectomy

Sponsors

The First Affiliated Hospital of Army Medical University, PLA
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Aged >= 18 years; 2.Symptoms indicative of acute ischemic stroke in the post-circulation phase, with an onset time (last known normal) within 24 hours (isolated vertigo is not considered a symptom of onset), confirmed by CTA, MRA, or DSA imaging to show basilar artery occlusion or intracranial vertebral artery occlusion (specifically, when the basilar artery is supplied solely by a unilateral vertebral artery). 3.Prestroke mRS score 0 or 1; 4.NIHSS score on admission >= 6; 5.Successful endovascular thrombectomy (eTICI 2b50-3); 6.The patient or their legal representative is able to understand the purpose of the trial, voluntarily participate, and sign a written informed consent form;

Exclusion criteria

Exclusion criteria: 1.Imaging data indicated the presence of intracranial hemorrhage or cerebellar infarction which exhibited a pronounced mass effect; 2.Baseline imaging examination revealed extensive infarcts in the posterior circulation region, as defined by PC-ASPECTS 3.0; 9.Platelet 185 mmHg or diastolic pressure >110 mmHg, and cannot be controlled by antihypertensive drugs; 11.Pregnant or lactating patients; 12.Life expectancy is less than 1 year; 13.Current participation in another clinical trial; 14.Neurologists do not consider other special circumstances appropriate for participation in this study;

Design outcomes

Primary

MeasureTime frame
Proportion of mRS score 0 to 1 at 90 (+/-7) days;

Secondary

MeasureTime frame
Proportion of mRS score 0 to 2 at 90 (+/-7) days;Proportion of mRS score 0 to 3 at 90 (+/-7) days;Shift in the distribution of mRS scores at 90 (+/-7) days;The change of the NIHSS score at 5–7 days after surgery or discharge ;European Quality Five-Dimension scale score at 90 (+/-7) days;symptomatic intracranial hemorrhage (sICH) within 48 h after treatment;All-cause mortality at 90 (+/-7) days;

Countries

China

Contacts

Public ContactZhenhua Zhou

The First Affiliated Hospital of Army Medical University, PLA

exploiter001@126.com+86 23 68765461

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026