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A register study to assess the effect of reduction disability for edarafen dextrocanol on ischemic stroke in real world

A register study to assess the effect of reduction disability for edarafen dextrocanol on ischemic stroke in real world - DEFEND

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200064340
Enrollment
Unknown
Registered
2022-10-03
Start date
2022-10-01
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

Ischemic stroke

Interventions

edarafen dextrocanol:Treating with edarafen dextrocanol

Sponsors

The First Hospital of Shanxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 120 Years

Inclusion criteria

Inclusion criteria: 1. Age was 18 years old; 2. Clinical diagnosis of acute ischemic stroke; 3. Have received the informed consent content and agreed to participate; 4. The stroke occurred from 72 hours to admission.

Exclusion criteria

Exclusion criteria: Exclusion criteria: 1. Patients during pregnancy or lactation or planned pregnancy within 90 days; 2. Patients with severe renal failure (eGFR <30 ml/min); 3. Patients with severe mental disorder or unable to complete informed consent and follow-up due to dementia; 4. Complicated malignancy or severe systemic disease with an expected survival of less than 90 days; 5. Have participated in other clinical intervention studies within 30 days before registration or are participating in other clinical intervention investigators.

Design outcomes

Primary

MeasureTime frame
Proportion of patients with mRS between 0 to 1 ;

Countries

China

Contacts

Public ContactXiaoyuan Niu

First Hospital of Shanxi Medical University

niuxiaoyuan1958@163.com+86 13303467183

Outcome results

None listed

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