Rivaroxaban for the Prevention of Deep Vein Thrombosis in Patients With Left Iliac Vein Compression - The PLICTS Study
NCT04067505 · Status: RECRUITING · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 224
Last updated 2024-04-18
Summary
The purpose of this study is to evaluate the efficacy and safety of rivaroxaban for the prevention of deep vein thrombosis in patients with left iliac vein compression treated with stent implantation.
Conditions
- May-Thurner Syndrome
Interventions
- DRUG
-
Rivaroxaban
Dose: 15mg twice daily for three weeks, then 20mg once daily until six months after the operation. Application: oral
- DRUG
-
Warfarin
Dose: 3mg for 5 days after the operation, later 0.75mg to 18mg depending on INR (2.0-3.0) until 6 months Duration: 6 months Frequency: once daily Application: oral
- DRUG
-
Nadroparin
Dose: 1mg/kg Duration: 5 days after the operation Frequency: twice daily Application: subcutaneous
Sponsors & Collaborators
-
Sir Run Run Shaw Hospital
collaborator OTHER -
Huadong Hospital
collaborator OTHER -
Shanghai Zhongshan Hospital
collaborator OTHER -
Shanghai 5th People's Hospital
collaborator OTHER -
Yantai Yuhuangding Hospital
collaborator OTHER -
Anhui Provincial Hospital
collaborator OTHER_GOV -
Zhejiang Provincial People's Hospital
collaborator OTHER -
Zhejiang Hospital
collaborator OTHER -
Second Affiliated Hospital, School of Medicine, Zhejiang University
lead OTHER
Principal Investigators
-
Zhejie Liu, MD,PhD · Second Affiliated Hospital, School of Medicine, Zhejiang University
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 75 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2020-05-18
- Primary Completion
- 2024-12-31
- Completion
- 2024-12-31
Countries
- China
Study Locations
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