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Effect of Butylphthalide on HGF Expression in Ischemic Stroke Patients

Effect of Butylphthalide on HGF Expression in Ischemic Stroke Patients

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OPN-17011341
Enrollment
Unknown
Registered
2017-05-09
Start date
2017-06-01
Completion date
Unknown
Last updated
2017-05-22

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

Conditions

Cerebral vascular structure, dysfunction and related diseases

Interventions

ctonrol group:Routine treatments for acute ischemic patients such as anti-platelet aggregation, anti-hypertension, lipid lowering, glycemic control depending on individual conditions.
NBP group:dl-3-n-butylphthalide, and also give routine treatments for acute ischemic stroke patients the same as control group.

Sponsors

The First Affiliated Hospital of Xinxiang Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
29 Years to 60 Years

Inclusion criteria

Inclusion criteria: All the cases were diagnosed in line with the Fourth National Conference of cerebrovascular disease diagnostic criteria adopted by the skull CT or MRI confirmed. TOAST etiology of atherosclerosis and small artery occlusion were patients. There was no significant poststroke dysfunction in the patients. The National Institutes of Health Stroke Scale (NIHSS) score was 2 to 12 (median, 6). Patients with severe visual acuity, hearing impairment, to complete the scale assessment, the better the compliance of the researchers. No severe systemic complications (such as various acute and chronic inflammation, connective tissue disease, cancer, atrial fibrillation, heart failure, respiratory failure, liver and kidney dysfunction, blood diseases, malignancies.

Exclusion criteria

Exclusion criteria: 1. before the onset of cognitive dysfunction and mental disorders, pregnancy, breast-feeding women; 2. Before the onset of use of folic acid, vitamin B6 and vitamin B12 and other drugs; 3. Patients who are in serious condition or unable to complete the medication and cognitive function scale due to disability; 4. Emergency thrombolysis or interventional therapy were excluded; 5. Subjects withdrawn from the standard: 5.1 It is necessary for the subject to discontinue the test for the study of drug allergy or the investigator's medical consideration. 5.2 The subject or his family request withdrawal test.

Design outcomes

Primary

MeasureTime frame
high-sensitivity C-reactive protein(hs-CRP);hepatocyte growth factor(HGF);Oxidized low-density lipoprotein(ox-LDL);Montreal cognitive assessment (MoCA);Minimum Mental State Examination;regional cerebral blood flows (rCBF);regional cerebral blood volume (rCBV);mean transit time (MTT);time to peak (TTP);

Countries

China

Contacts

Public ContactZhang Ping

The First Affiliated Hospital of Xinxiang Medical University

zhangpingsjnk@163.com+86 13673732099

Outcome results

None listed

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