Trials
Search / Trial NCT06428110

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.

Locations

Shanghai, Shanghai, China

People applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

Discussion 0