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Study on the interaction between traditional Chinese medicine and new oral anticoagulant drugs in cardiovascular diseases and its clinical application

Study on the interaction between traditional Chinese medicine and new oral anticoagulant drugs in cardiovascular diseases and its clinical application

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400086299
Enrollment
Unknown
Registered
2024-06-28
Start date
2025-10-25
Completion date
Unknown
Last updated
2025-10-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

patients that need for anticoagulation therapy

Interventions

NOACs monotherapy group:None
Herb-NOACs combination group:None

Sponsors

Beijing Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: (1) the clinic patients need for anticoagulation with NVAF, venous thromboembolism, pulmonary embolism, etc.; (2) age >= 18 years old, male or female; (3) NOACs group (control group) or target herb and NOACs combination group (exposure group) were treated for 3-6 months; (4) the patient is willing and able to cooperate to accept follow-up.

Exclusion criteria

Exclusion criteria: (1) patient with combined immunodeficiency diseases; (2) patient has a history of chronic liver disease, hepatitis b surface antigen and/or hepatitis c antibody positive; (3) NOACs taboo certificate (including severe liver and kidney function was abnormal, blood coagulation was abnormal, obvious active bleeding, bleeding, significant risk lesions or disease, severe hypertension, anticoagulants with healers, pregnant women and nursing mothers); (4) NOACs within 14 days before treatment used potent CYP3A4 inhibitors and/or P - gp inhibitors, potent CYP3A4 inducers and/or P - gp inducers; (5) unable to obtain the necessary clinical data; (6) There were other conditions that the researchers considered inappropriate for participation.

Design outcomes

Primary

MeasureTime frame
Outcome events: including bleeding events (including major bleeding, clinically relevant non major bleeding, minor bleeding), stroke/systemic embolism events;

Countries

China

Contacts

Public ContactPengfei Jin

Beijing Hospital

j790101@163.com+86 138 1130 0092

Outcome results

None listed

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