A Prospective Cohort Study on Warfarin Personalized Medication
Launched by HAOBIN LI · May 20, 2024
Trial Information
Current as of February 18, 2025
Completed
Keywords
ClinConnect Summary
No description provided
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Patients aged 65 years and older, taking warfarin, with or without premature vascular aging, regardless of gender.
- • Patients who have not concurrently or intermittently used anticoagulant drugs, including antiplatelet drugs, heparin, low molecular weight heparin, and non-vitamin K-dependent oral anticoagulants, such as dabigatran and apixaban.
- • Signing an informed consent form before blood sample collection.
- Exclusion Criteria:
- • Patients who are allergic to warfarin or lactose.
- • Patients who are receiving immunosuppressive agents or low molecular weight heparin anticoagulants.
- • Patients with bleeding tendencies, blood disorders with platelet counts \> 400 × 10\^9 /L or \< 100 × 10\^9 /L, hemoglobin \> 169 or \< 100 g/L.
- • History of peptic ulcer disease.
- • Malignant tumors, severe multi-organ dysfunction or failure such as heart, liver, and kidney.
- • Neurological disorders such as epilepsy.
Trial Officials
Guangchun Sun
Principal Investigator
The Fifth People's Hospital of Shanghai
About Haobin Li
Haobin Li is a dedicated clinical trial sponsor focused on advancing medical research and improving patient outcomes through innovative study designs and rigorous methodologies. With a commitment to ethical standards and regulatory compliance, Haobin Li collaborates with healthcare professionals and research institutions to conduct high-quality clinical trials across various therapeutic areas. By fostering transparency and collaboration, Haobin Li aims to contribute to the development of safe and effective treatments, ultimately enhancing the quality of care in the healthcare community.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Shanghai, Shanghai, China
People applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
Discussion 0