Skip to content

The efficacy and safety of Cattle encephalon glycoside and ignotin in the treatment of brain damage of patients with acute cerebral infarction: A Randomized, double-blind, parallel-group, placebo-controlled trial

The efficacy and safety of Cattle encephalon glycoside and ignotin in the treatment of brain damage of patients with acute cerebral infarction: A Randomized, double-blind, parallel-group, placebo-controlled trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800017937
Enrollment
Unknown
Registered
2018-08-23
Start date
2013-11-18
Completion date
Unknown
Last updated
2018-08-27

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

Conditions

Acute Cerebral Infarction

Interventions

CEGI group:All patients were given standard care once daily for 14 days, including oral 200g aspirin enteric-coated tablet and 20 mg atorvastatin calcium, and intravenous infusion of 250~500 ml 0.9% s
Placebo group:All patients were given standard care once daily for 14 days, including oral 200g aspirin enteric-coated tablet and 20 mg atorvastatin calcium, and intravenous infusion of 250~500 ml 0.9

Sponsors

Peking University Third Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. those diagnosed with first-ever acute cerebral infarction within 48 hours of onset or relapsed ischemic stroke with a score of 0-1 on modified Rankin Scale (mRS); 2. aged between 18 and 75 years old; 3. had a score of 5-22 points on the National Institutes of Health Stroke Scale (NIHSS); and (d) signed informed consent form.

Exclusion criteria

Exclusion criteria: 1. they were diagnosed with transient ischemic attack (TIA), non-responsible multi lacunar infarction, cerebral hemorrhage after infarction, subarachnoid hemorrhage, and/or post-circulation ischemia; 2. had hemiplegia caused by brain tumor, brain injury, brain parasitic diseases and metabolic disorder, cerebral embolism caused by rheumatic heart disease, coronary heart disease, or other heart disease with atrial fibrillation; 3. had gangliosidoses (such as Familial Mongolian idiocy); 4. thrombolytic patients or peptic ulcer patients who cannot take aspirin; 5. had severe primary disease of cardiovascular, liver (ALT or AST exceeding a 1.5-fold upper range value), renal (blood urea nitrogen (BUN) exceeding a 1.2-fold upper range value , creatinine exceeding a 2-fold upper range value), hematopoietic, and/or endocrine system; 6. presented allergies to the study drug or protein; 7. depended on drug or alcohol; 8. pregnant or lactating women; 9. participated in other clinical trials within the past 3 months.

Design outcomes

Primary

MeasureTime frame
mRS on day 90;

Secondary

MeasureTime frame
NIHSS;Barthel Index scores;

Countries

China

Contacts

Public ContactZhang Hui

Peking University Third Hospital

liuping831120@yeah.net+86 18910739566

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 19, 2026