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
| Type | Name | Description |
|---|---|---|
| DRUG | Rivaroxaban 10 MG | Rivaroxaban pill 10mg qd, day1 and day2 after femoral venepuncture |
| DRUG | Rivaroxaban 20 MG | Rivaroxaban pill 10mg bid, day1 and day2 after femoral venepuncture |
| DRUG | Low-molecular-weight heparin | 0.4 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.