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Clinical Study on Floium Ginkgo Extract and Tertram Ethypyrazine Sodium Chloride injection in Treatment of Acute Ischemic Stroke

Clinical Study on Floium Ginkgo Extract and Tertram Ethypyrazine Sodium Chloride injection in Treatment of Acute Ischemic Stroke

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR1900002858
Enrollment
Unknown
Registered
2019-12-20
Start date
2019-12-21
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

acute ischemic stroke

Interventions

Sponsors

The First Hospital of China Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) aged >= 18 years; 2) acute ischemic stroke patients with first symptom onset; 3) symptom onset within 4.5 hours and eligible for criteria for IV-tPA treatment; 4) baseline NIHSS score range from 7 to 22; 5) written informed consent has been provided by patients or their legal proxies.

Exclusion criteria

Exclusion criteria: 1) Allergic to the drug components in this study. 2) Oral or intravenous application of other drugs similar to the mechanism of Floium Ginkgo Extract and Tertram Ethypyrazine Sodium Chloride injection before stroke onset(28 days). 3) Epilepsy with stroke onset. 4) Other lesions in the brain, history of mental illness. 5) History of chronic liver disease, liver and kidney dysfunction, elevated alanine aminotransferase (> 3 times the upper limit of normal), and elevated serum creatinine (> 2 times the upper limit of normal). 6) Pregnant or lactating women. 7) Other severe, advanced or terminal illnesses with life expectancy of less than 3 months, or inability to complete study follow-up due to other reasons. 8) Other circumstances that the researchers consider not appropriate for this study.

Design outcomes

Primary

MeasureTime frame
reperfusion improvement;

Secondary

MeasureTime frame
Rate of adverse events;Vascular recanalization;Ischemic penumbra;proportion of patients with a mRS score of 0-2;Proportion of patients with a NIHSS score at day 15, day 30, day 90 of 0-1 or a reduction of = 8 points from baseline;proportion of patients with a Barthel score=95;

Countries

China

Contacts

Public ContactChuansheng Zhao

The First Hospital of China Medical University

zhaocs@cmu1h.com+86 13940369251

Outcome results

None listed

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