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Clinical Study on In-hospital Anticoagulant Therapy for Pulmonary Embolism monitored by Anti-factor Xa level

Clinical Study on In-hospital Anticoagulant Therapy for Pulmonary Embolism monitored by Anti-factor Xa level

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500107616
Enrollment
Unknown
Registered
2025-08-15
Start date
2025-08-15
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Pulmonary Thromboembolism(PTE)

Interventions

Group A:Adjust the dosage of heparin or low molecular weight heparin based on anti-factor Xa level
Group B:Patients receiving heparin anticoagulation will have their heparin dosage adjusted according to activated partial thromboplastin time (APTT), while those receiving low molecular weight heparin

Sponsors

Fuwai Hospital, Chinese Academy of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.>=18 years old; 2. Patients with acute pulmonary embolism who were initially diagnosed; 3. Signed informed consent and agreed to receive heparin/low molecular weight heparin anticoagulation therapy.

Exclusion criteria

Exclusion criteria: 1. Previous history of pulmonary embolism 2. Patients cannot sign the informed consent form or cannot cooperate with the completion of the study. 3. Those who are allergic to heparin/low molecular weight heparin. 4. Previous heparin/low molecular weight heparin-induced thrombocytopenia (HIT) or heparin/low molecular weight heparin-induced of patients with a history of thrombocytopenia with thrombosis (HITT). 5. Severe bleeding disorders

Design outcomes

Primary

MeasureTime frame
Post-Pulmonary Embolism Syndrome;

Secondary

MeasureTime frame
Incidence of bleeding events from initial anticoagulation to 3 months of follow-up;

Countries

China

Contacts

Public ContactYou Lingyan

Fuwai Hospital, Chinese Academy of Medical Sciences

Youlingyan@fuwai.com+86 152 8049 1856

Outcome results

None listed

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