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Screening of genes associated with bleeding and evaluation of the risk of bleeding after the treatment of anti-thrombosis

Screening of genes associated with bleeding and evaluation of the risk of bleeding after the treatment of anti-thrombosis

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ROC-16010050
Enrollment
Unknown
Registered
2016-11-30
Start date
2016-12-05
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

Aspirin group:Aspirin, 100mg, qd
Clopidogrel Group:Clopidogrel 75mg, qd
Aspirin+Clopidogrel Group:Aspirin, 100mg, qd+Clopidogrel,75mg, qd
Warfarin Group:Warfarin, INR 2-2.5
Pradaxa Group:Pradaxa 150mg, bid

Sponsors

Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-80 year old patients with acute ischemic stroke; 2. onset within 72 hours, cerebral infarction confirmed by head MR and CT scan, without cerebral hemorrhage or micro hemorrhage; 3. signed informed consent and able to cooperate with follow-up.

Exclusion criteria

Exclusion criteria: 1. history of intracranial hemorrhage or subarachnoid hemorrhage; 2. with hemorrhagic transformation after cerebral infarction this time; 3. the survival of patients was less than 1 year; 4. with contraindications to antithrombotic therapy, or allergy to related drugs; 5. serious heart, liver or renal insufficiency patients; 6. with severe pulmonary or systemic infection; 7. with other brain organic diseases, such as brain tumors, cerebral aneurysm, intracranial vascular malformations, et al; 8. participated in other clinical researches within 3 months; 9. HIV positive, syphilis antibody positive, hepatitis B or hepatitis C patients; 10. with severe mental disorders, cognitive dysfunction, or cant understand and sign the informed consent; 11. with coagulation dysfunction, active or tendency to bleeding; 12. with high blood pressure difficult to control, severe diabetes or other diseases affect the function of the limb.

Design outcomes

Primary

MeasureTime frame
NIHSS;mRS;ADL;HRQoL;MOCA;CDT;

Countries

China

Contacts

Public ContactYUN XU

Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing

xuyun20042001@aliyun.com+86 025 83105208

Outcome results

None listed

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