MedTrace Logo

A Multi-Center Study to Evaluate Acute Safety and Clinical Performance of Paladin® Carotid Post-Dilation Balloon System With Integrated Embolic Protection

NCT02501148 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 106

Last updated 2022-11-21

No results posted yet for this study

Summary

The purpose of this study is to assess the safety and clinical performance of Paladin System in patients with carotid artery stenosis.

Conditions

  • Carotid Artery Stenoses

Interventions

DEVICE

carotid artery stenting

Post-dilation of deployed self-expanding carotid stent with the Paladin Post-Dilation Balloon System with Integrated Embolic Protection

Sponsors & Collaborators

  • Contego Medical, Inc.

    lead INDUSTRY

Principal Investigators

  • Prof. Thomas Zeller, MD · Universitäts Herzzentrum Freiburg Bad-Krozingen

  • Prof. Horst Sievert, MD · CardioVascular Center, Sankt Katharinen Hospital

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-08-31
Primary Completion
2016-09-30
Completion
2016-10-31

Countries

  • Germany

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 NCT02501148 on ClinicalTrials.gov