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A multicenter clinical trial assessment of Baiyu Ginkgolide injection, in the treatment of ischemic stroke with blood stasis syndrome

A multicenter clinical trial assessment of Baiyu Ginkgolide injection, in the treatment of ischemic stroke with blood stasis syndrome

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ONC-13003247
Enrollment
Unknown
Registered
2013-05-27
Start date
2013-06-01
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

Ischemic Stroke

Interventions

test group:Baiyu Ginkgolide injection

Sponsors

The Second Affiliated Hospital of Tianjin University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 100 Years

Inclusion criteria

Inclusion criteria: 1. patients accord to diagnostic standards on western medical ischemic stroke; 2. patients accord to diagnostic standards on Chinese medical attack to meridians; 3. 7 days to 6 months after invasion; 4. patients accord to differentiation standards on blood stasis syndrome; 5. patients must be voluntary to be subjected and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. patients accompany with unconsciousness or severe dementia; 2. patients allergic to Ginkgo biloba drugsethanol or glycerin; 3. patients who are pregnant,nursing or planning for pregnancy; 4. patients with hemorrhagic cerebral infarction and cerebral arteritis; 5. patients with cerebral embolism caused by cerebral tumor,trauma,parasitosis,rheumatic heart disease,coronary heart disease and other heart disease complicated with atrial fibrillation; 6. ALT, AST>=2.5 times of upper limit of normal, Cr>=1.5 times of upper limit of normal; 7. patients with insanity or not suitable for clinical trial under doctors' consideration; 8. patients with hemorrhagic tendency, severe bleeding within 3 months, PLT under lower limit of normal or APTT above 3 seconds of control value; 9. patients who have participated in other clinical trial in 1 month.

Design outcomes

Primary

MeasureTime frame
Adverse Events;BP, temperature, breath, heart rate;blood routine, urine routine, stool routine +occult;ALT, AST, TBIL, ALP, garma-GT, BUN, Cr, beta2-MG;CK, CK-MB;PT, APTT, TT, FIB, D-Dimer;ECG;

Countries

China

Contacts

Public ContactBaohe Wang
wbh3423@sina.com+86 022 60335386

Outcome results

None listed

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