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A multicenter registry study of distal medium vessel occlusion stroke

A multicenter registry study of distal medium vessel occlusion stroke

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500096954
Enrollment
Unknown
Registered
2025-02-10
Start date
2024-03-05
Completion date
Unknown
Last updated
2025-02-17

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

Conditions

Cerebrovascular disease

Interventions

Observation group:None

Sponsors

Department of Neurology, The First Affiliated Hospital of University of Science and Technology of China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1. Age>=18 years; 2. Pre-stroke mRS<=2; 3. Evidence of distal medium vascular occlusion defined as occlusion of the non-dominant M2 segment* /M3/M4segment of the MCA, the ACA (A1, A2, or A3 segments), or the PCA (P1, P2 or P3 segments) confirmed by CTA/MRA/DSA; 4.Time from symptom onset to treatment <24 hours; 5.Informed consent obtained from patient or acceptable patient surrogate.

Exclusion criteria

Exclusion criteria: 1) neuroimaging evidence of cerebral hemorrhage on presentation; 2) patients who had primary proximal large vessel occlusion, multivessel occlusion, missing baseline mRS scores, or missing clinical variables were excluded from the analysis. 3) serious, advanced, or terminal illness.

Design outcomes

Primary

MeasureTime frame
Modified Rankin Scale (mRS) score at 90 days;Symptomatic intracranial hemorrhage at 24 hours;

Secondary

MeasureTime frame
Mortality at 90 days;Ratio of 90-day mRS <= 2 or 90-day mRS <= 1;

Countries

China

Contacts

Public ContactWei Hu

Department of Neurology, The First Affiliated Hospital of University of Science and Technology of China

ahslyykyc@163.com+86 151 5551 0611

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 10, 2026