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Safety and Efficacy of SYM-SV/DS-002 in Patients With Severe Aortic Stenosis

NCT03004599 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 11

Last updated 2017-11-06

No results posted yet for this study

Summary

Safety and Efficacy of SYM-SV/DS-002 in Patients with Severe Aortic Stenosis

Conditions

  • Severe Aortic Stenosis

Interventions

DEVICE

SYM-SV-002 Aortic Bioprosthesis and SYM-DS-002 Transfemoral Delivery System

Transcatheter Aortic Valve Implantation via Transfemoral Approach

Sponsors & Collaborators

  • Medico's Hirata Inc.

    lead OTHER

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-11-30
Primary Completion
2017-10-31
Completion
2017-10-31

Countries

  • Japan

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03004599 on ClinicalTrials.gov