Peripheral Venous Stent System in the Treatment of Iliac Vein Stenosis or Occlusion
- Conditions
- Iliac Vein OcclusionIliac Vein Stenosis
- Registration Number
- NCT04812444
- Lead Sponsor
- Zhejiang Zylox Medical Device Co., Ltd.
- Brief Summary
Clinical study on safety and efficacy of Zylox peripheral venous stent system in the treatment of iliac vein stenosis or occlusion.
- Detailed Description
The purpose of this study was to evaluate the safety and efficacy of Zylox peripheral venous stent system in the treatment of iliac vein stenosis or occlusive lesions compare with conventional venous stent.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 220
- Aged from 18 to 75 years old, male or female
- Subject's target lesions were stenosis and/or occlusion
- CEAP≥C3
- Subjects were able to understand the purpose of the study, demonstrate full compliance with the program and sign informed consent
- Pregnant woman or who's pregnancy test is positive
- Lactation period woman or woman/man with fertility plan
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Target vascular patency rate at 12 months after operation 12 months Target vascular patency rate
- Secondary Outcome Measures
Name Time Method Adverse Event Preoperative、Intraoperative、up to 1 month、3 month、6 month、12 month、2 years、3 years、5 years Adverse medical events,whether or not related to the medical device
The incidence of major adverse events 12 months Related to death of clinical trials
Related Research Topics
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Trial Locations
- Locations (1)
The First Affiliated Hospital of Chongqing Medical University
🇨🇳Chongqing, Chongqing, China
The First Affiliated Hospital of Chongqing Medical University🇨🇳Chongqing, Chongqing, China