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Fondaparinux in the prevention of venous thromboembolism in patients with respiratory diseases: a multicenter, prospective, randomized, controlled trial

Fondaparinux in the prevention of venous thromboembolism in patients with respiratory diseases: a multicenter, prospective, randomized, controlled trial

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000035406
Enrollment
Unknown
Registered
2020-08-10
Start date
2020-07-31
Completion date
Unknown
Last updated
2020-08-17

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

Conditions

Chronic obstructive pulmonary disease (COPD), lung cancer, interstitial lung disease, pneumonia

Interventions

Fondaparinux sodium:5 mg, QD, subcutaneous injection, 7-14 days.
Low molecular weight heparin:4000 axaiu (0.4 ml), QD, subcutaneous injection, 7-14 days

Sponsors

Tianjin Medical University General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Hospitalized patients with respiratory diseases over 18 years old; 2. Patients who need anticoagulant drugs to prevent VTE according to Padua score >= 4; 3. Patients or legal representatives have been informed of the nature of the study and understand the provisions in the protocol to ensure compliance.

Exclusion criteria

Exclusion criteria: 1. Allergy or contraindication to fondaparinux and enoxaparin; 2. High risk of bleeding: patients or history of hemorrhagic diseases, bleeding tendency, bleeding constitution or coagulation disorders; 3. Patients with hyperthyroidism and severe hepatic and renal insufficiency were contraindicated; 4. Having participated in the research of other drugs / devices or during the follow-up period of another drug / device research; 5. Patients may not comply with the research protocol (including the follow-up period), such as mental disorders, alcohol or drug abuse, etc..

Design outcomes

Primary

MeasureTime frame
7-day thrombotic events (including lower extremity deep vein thrombosis, pulmonary embolism, and intraductal thrombosis);7-day bleeding event (any bleeding event, thrombocytopenia);

Secondary

MeasureTime frame
30 day bleeding events;

Countries

China

Contacts

Public ContactJie Cao

General Hospital of Tianjin Medical University

tjcaojie@sina.com+86 13132088076

Outcome results

None listed

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