Skip to content

Prospective Research of the Relationship between the Rehabilitative Prognosis and the Intensive Atorvastatin Therapy on Acute Cerebral Infarction.

Prospective Research of the Relationship between the Rehabilitative Prognosis and the Intensive Atorvastatin Therapy on Acute Cerebral Infarction.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OOC-15006888
Enrollment
Unknown
Registered
2015-07-13
Start date
2015-08-05
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Cerebrovascular Disease

Interventions

intensive group:atrovastatin 80mg×14day
control group:atrovastatin 20mg×14day

Sponsors

Beijing Luhe Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Acute ischemic stroke patients with new focal neuro-signs should be proved new infarction lesions exist by CT/MRI. Patients' disease time should be less than 24 hours or they have advancing stroke. Patients who agree to take the trial should sign the informed consents first.

Exclusion criteria

Exclusion criteria: Patients whose ages are less than 18 years or more than 80 years will not be included. Patients whose liver founction or creatine kinase is apparently abormal will not be included.Patients who have serious heart diseases, cancers, allergy to atorvastatin, difficulties of follow-up or life expectancy less than 1 year will not be included. Patients who refuse sign the informed consents will also be excluded.

Design outcomes

Primary

MeasureTime frame
NIHSS Score;

Countries

China

Contacts

Public ContactTAN XIAOMU
yztxm@sina.com.cn+86 15901197855

Outcome results

None listed

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