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Prospective Randomized Trial on Efficacy of Rivaroxaban and Wafarin on Preventing Vein Thromboembolism in Nephrotic Syndrome

Prospective Randomized Trial on Efficacy of Rivaroxaban and Wafarin on Preventing Vein Thromboembolism in Nephrotic Syndrome

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000029081
Enrollment
Unknown
Registered
2020-01-13
Start date
2021-01-15
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

Nephrotic Syndrome

Interventions

Rivaroxaban Preventing Group:10mg/d Rivaroxaban on preventing vein thromboembolism
Warfarin Preventing Group:Warfarin targeting INR 2-3 on preventing vein thromboembolism

Sponsors

Peking Union Medical College Hospital, Chinese Academy of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Age: 18-80 years old; (2) Qualitative diagnosis: clinical diagnosis of nephropathy syndrome; (3) At least one of the following high coagulation tendencies combined: plasma albumin less than 25 g/L, membrane nephropathy, past history of venous thrombosis, a family history of venous thrombosis; (4) Calculated glomerular filtration rate more than 30 ml/min; (5) The patient and family members understand the purpose of the research well and are willing to participate in the study and provide written informed consent.

Exclusion criteria

Exclusion criteria: (1) Cancer with expected survival period fewer than 6 months; (2) Serious liver disease; (3) Surgery is required in the near future; (4) Pregnant or lactating women; (5) Vascular ultrasound examination found that there is an existing venous thrombosis; (6) Contraindication of anticoagulation treatment of Rivaroxaban or Warfarin.

Design outcomes

Primary

MeasureTime frame
Combined incidence of bleeding events (including mild and severe bleeding events) and thrombosis events within 6 months after anticoagulant treatment;

Secondary

MeasureTime frame
Cost of anticoagulant-related therapy within 6 months after anticoagulant therapy;Complete and partial remission rate of nephrotic syndrome within 6 months after anticoagulant treatment;

Countries

China

Contacts

Public ContactChen Gang

Peking Union Medical College Hospital, Chinese Academy of Medical Science

chengang@pumch.cn+86 18600112886

Outcome results

None listed

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