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Rivaroxaban versus Fondaparinux Observational Study for Thromboprophylaxis After Hip or Knee Arthroplasty

Rivaroxaban versus Fondaparinux Observational Study for Thromboprophylaxis after Hip or Knee Arthroplasty

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2017/10/010059
Enrollment
100
Registered
2017-10-12
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: Z471- Aftercare following joint replacement surgery Health Condition 2: null- Patients undergoing elective knee or hip surgery

Interventions

None listed

Sponsors

Virchow Biotech Private Limited
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Male or Female patients who are undergoing elective hip or knee replacement surgery

Exclusion criteria

Exclusion criteria: Patients with active bleeding or a high risk of bleeding that contraindicated the use of rivaroxaban ; Other exclusion criteria included conditions preventing bilateral venography, clinically significant liver, cardiac, renal disease, concomitant use of protease inhibitors of the human immunodeficiency virus or fibrinolytic agents, planned intermittent pneumatic compression, requirement of ongoing anticoagulant therapy, and pregnancy or breast-feeding.

Design outcomes

Primary

MeasureTime frame
Any Major BleedingTimepoint: 3 months

Secondary

MeasureTime frame
Any Minor BleedingTimepoint: 3 months

Countries

India

Contacts

Public ContactDr Hemanth Nandigala

Virchow Biotech Private Limited

hnandigala@gmail.com040-64581006

Outcome results

None listed

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