New Covered Stent (Willis) for the Endovascular Reconstruction of Intracranial Vessel Wall Defects Registry
NCT02820779 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100
Last updated 2016-07-01
Summary
The purpose of this study is to evaluate the effectiveness, long-term safety and explore the safety and efficacy factors WILLIS™ intracranial stent graft system in clinical applications.
Conditions
- Aneurysm, Intracranial
- Carotid-Cavernous Sinus Fistula
Interventions
- DEVICE
-
WILLIS
WILLIS® intracranial stent graft system is composed of the stent, delivery system, cobalt-based alloy stent and PTFE graft. It can effectively shunt the blood flow and keep it off of the aneurysm wall.
Sponsors & Collaborators
-
First Affiliated Hospital of Harbin Medical University
collaborator OTHER -
The Second Affiliated Hospital of Harbin Medical University
collaborator OTHER -
Qilu Hospital of Shandong University
collaborator OTHER -
Shanghai Tongji Hospital, Tongji University School of Medicine
collaborator OTHER -
Nanfang Hospital, Southern Medical University
collaborator OTHER -
Tang-Du Hospital
collaborator OTHER -
West China Hospital
collaborator OTHER -
The First Affiliated Hospital of Zhengzhou University
collaborator OTHER -
Shaanxi Provincial People's Hospital
collaborator OTHER -
Shandong Provincial Hospital
collaborator OTHER_GOV -
First Affiliated Hospital of Xinjiang Medical University
collaborator OTHER -
Xuanwu Hospital, Beijing
lead OTHER
Principal Investigators
-
Hongqi Zhang, MD · [email protected]
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2016-06-30
- Primary Completion
- 2019-05-31
- Completion
- 2019-05-31
Countries
- China
Study Locations
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