Assessment of the St Jude Medical Portico Resheathable Aortic Valve System-Alternative Access

NCT03056573 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 64

Last updated 2025-02-11

Study results available
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Summary

Expand the indication of the Portico TF Delivery System and obtain approval of the Alternative Access Delivery System

Conditions

  • Aortic Valve Stenosis

Interventions

DEVICE

Transaortic TAVR Implant

Transaortic TAVR implant

DEVICE

Subclavian /Axillary TAVR implant

Subclavian /Axillary TAVR implant

Sponsors & Collaborators

  • Abbott Medical Devices

    lead INDUSTRY

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-03-29
Primary Completion
2018-12-31
Completion
2019-07-05

Countries

  • Denmark
  • Germany
  • Italy
  • Netherlands
  • Switzerland

Study Locations

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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 NCT03056573 on ClinicalTrials.gov