CLaret Embolic Protection ANd TAVI - Trial
NCT01833052 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100
Last updated 2015-05-05
Summary
This prospective, randomized study was designed to investigate the benefit of using a Filter-Protection-Device (Claret MontageTM Dual Filter System) during transcatheter aortic valve implantation (TAVI) with a Medtronic CoreValve®.
Conditions
- Frequency of Cerebral Perfusion Defects After TAVI
- Size of Cerebral Perfusion Defects After TAVI
Interventions
- DEVICE
-
TAVI (Medtronic CoreValve)
- DEVICE
-
Claret-Filter
Sponsors & Collaborators
-
University of Leipzig
lead OTHER
Study Design
- Allocation
- RANDOMIZED
- Purpose
- SUPPORTIVE_CARE
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2013-04-30
- Primary Completion
- 2014-06-30
- Completion
- 2015-06-30
Countries
- Germany
Study Locations
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