Clinical Trials Directory

Trials / Completed

CompletedNCT03282643

Rivaroxaban Versus Low-molecular-weight Heparin for Preventing Thrombosis in Cancer Patients

Rivaroxaban Versus Low-molecular-weight Heparin in Preventing Thrombosis Among Cancer Patients After Femoral Venepuncture

Status
Completed
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
74 (actual)
Sponsor
Capital Medical University · Academic / Other
Sex
All
Age
18 Years – 85 Years
Healthy volunteers
Not accepted

Summary

The study is designed to compare the efficacy and safety of oral rivaroxaban and subcutaneous low-molecular-weight heparin in preventing femoral venepuncture associated thrombosis among cancer patients.

Conditions

Interventions

TypeNameDescription
DRUGRivaroxaban 10 MGRivaroxaban pill 10mg qd, day1 and day2 after femoral venepuncture
DRUGRivaroxaban 20 MGRivaroxaban pill 10mg bid, day1 and day2 after femoral venepuncture
DRUGLow-molecular-weight heparin0.4 ml once daily, before femoral venepuncture(day1) and the following day (day 2)

Timeline

Start date
2016-02-16
Primary completion
2018-06-30
Completion
2019-04-01
First posted
2017-09-14
Last updated
2019-04-16

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT03282643. Inclusion in this directory is not an endorsement.

Rivaroxaban Versus Low-molecular-weight Heparin for Preventing Thrombosis in Cancer Patients (NCT03282643) · Clinical Trials Directory