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Construction of a prospective cohort database for genetic thrombosis gene stratification and exploration of the efficacy and safety of NOACs treatment strategies

Construction of a prospective cohort database for genetic thrombosis gene stratification and exploration of the efficacy and safety of NOACs treatment strategies

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500115214
Enrollment
Unknown
Registered
2025-12-23
Start date
2025-12-25
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Hereditary venous thromboembolism

Interventions

Sponsors

Shanghai General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >= 18 years old; 2. Diagnosis of VTE (DVT/PE); 3. Genetic testing confirmed the presence of hereditary thrombophilia (such as F5/F2 mutations or defects in natural anticoagulant proteins); 4. Plans to undergo long-term treatment with NOACs (rivaroxaban/edoxaban/dabigatran) for more than 6 months; 5. Can understand and sign the informed consent form, and are willing to cooperate throughout the entire research process.

Exclusion criteria

Exclusion criteria: 1. Active bleeding or contraindications to anticoagulation; 2. Severe liver and kidney dysfunction (CrCl < 30 ml/min); 3. Pregnancy or lactation period; 4. Expected survival period < 6 months;

Design outcomes

Primary

MeasureTime frame
Recurrent thrombosis rate;

Secondary

MeasureTime frame
The incidence rate of major bleeding events;

Countries

China

Contacts

Public ContactYan Zhou

Shanghai General Hospital

nyyxzy@163.com+86 21 3779 8317

Outcome results

None listed

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