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A Safety and Effective Study of Ginkgolides Diterpene Lactone Meglumine Injection in the Treatment of Ischemic Stroke.

A Randomized,Double Blind,Placebo Parallel Controlled,Multicenter Clinical Sthdy of Ginkgo Diterpene Lactone Meglumine Injection for Acute Ischemic Stroke Efficacy Safety.

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02526225
Enrollment
3452
Registered
2015-08-18
Start date
2016-02-01
Completion date
2019-08-31
Last updated
2023-03-30

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

Conditions

Ischemic Stroke

Keywords

acute ischemic stroke, safety and effectiveness, Ginkgo diterpene lactone meglumine injection

Brief summary

The aim of this study is to evaluate the safety and effectivity of Ginkgo diterpene lactone meglumine injection tn the treatment of acute ischemic stroke

Detailed description

After randomized to 90 + 7 days mRS 0-1 points is the Primary Outcome Measure,evaluate the safety and effectivity of Ginkgo diterpene lactone meglumine injection tn the treatment of acute ischemic stroke

Interventions

5 ml/times, 1 time/day.Before use, the drug slowly added to the 0.9% sodium chloride injection diluted in 250 ml, slow intravenous drip.

5 ml/times, 1 time/day.Before use, the drug slowly added to the 0.9% sodium chloride injection diluted in 250 ml, slow intravenous drip.

Sponsors

Beijing Bionovo Medicine Development Co., Ltd.
CollaboratorOTHER
Beijing Tiantan Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. Aged 18 to 80 years of age, and gender not limited。 2. Within 48 hours of stroke onset of ischemic stroke (diagnosis standard by the Chinese medical association of the fourth national conference on cerebrovascular disease); 3. The first onset, or always not obvious legacy of stroke sequela (mRS acuities were before the onset of 1); 4. The degree of nerve function defect score (NIHSS) score 4 to 24 points, body movement component (NIHSS score paragraphs 5 and 6) total score 2 points or higher; 5. Understand and voluntarily signed informed consent.

Exclusion criteria

1. Head imaging studies have confirmed that, encephalitis, brain tumor, brain abscess and cause similar symptoms of disease, or confirm with hemorrhagic cerebral infarction, epidural hematoma, intracranial hematoma, intraventricular hemorrhage, subarachnoid hemorrhage, etc. 2. The serious disturbance of consciousness (Ia NIHSS score 2 points or higher); 3. With hemorrhagic disease or have a bleeding tendency, or have a lower limb venous thrombosis; 4. Serious abnormal liver and kidney function, liver function laboratory indexes of ALT \> 3 ULN, renal laboratory ULN Cr \> 1.5); 5. A history of mental illness or dementia patients; 6. Severe organ or other systemic disease, accompanied by any organ or system of malignant tumor, or ongoing anti-tumor treatment, the estimated lifetime \< 3 months; 7. Significant drug or alcohol abuse; 8. Allergic constitution, as well as to two or more drugs or food allergies;This medicine ingredients allergy or known; 9. Have pregnancy (check blood HCG positive screening tests, namely HCG \> 5 miu/mL), during the test preparation is pregnancy or lactation in women; 10. In the past three months in other clinical trials; 11. Researchers do not determine poor adherence, or any other suitable for patients to participate in this study.

Design outcomes

Primary

MeasureTime frame
Proportion of patients with Modified Rankin Scale (mRS) less than or equal to 1 .90 days

Secondary

MeasureTime frame
Proportion of patients with National Institutes of Health Stroke Score (NIHSS) reducing 4 points or more changes from baseline to randomized 7 days,14 days.Baseline,7 days,14 days,
Proportion of patients with Modified Rankin Scale (mRS) reaching 0-2 .90 days
The Montreal Cognitive Assessment (MoCA) scale changes from baseline to randomized 14 days,90 days.Baseline,14 days,90 days
Proportion of patients with National Institutes of Health Stroke Score (NIHSS) rising 4 or more points, three points, two points, one of the subjects changes from baseline to randomized 7 days.Baseline, 7days
The all-cause mortality90 days
Ischemic stroke recurrence rate90 days
Composite incidence of vascular events90 days
The EuroQol-5 Dimensions (EQ-5D) scale changes from baseline to randomized 14 days,90 days.Baseline,14 days,90 days

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 8, 2026