venous thromboembolism
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Voluntary signature of informed consent; aged 18 and 75 years old; diagnosis of VTE patients.
Exclusion criteria
Exclusion criteria: Patients with a history of ischemic cardiomyopathy, including myocardial infarction, symptomatic coronary artery disease within 6 months before admission to the clinical trial, cancer patients with VTE, emotional instability or intellectual inability to understand the objectives, nature of the study and the consequences of participating in the study, or any other possible unacceptable safety that the researchers consider unacceptable Whole risk situation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Gene polymorphism; | — |
Secondary
| Measure | Time frame |
|---|---|
| Peak Drug Concentration of Dapigatron Ester;Tough Drug Concentration of Dapigatron Ester;Peak drug concentration of Rivaroxaban;Tough drug concentration of Rivaroxaban; | — |
Countries
China
Contacts
Shanghai Pulmonary Hospital