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Registry of the Magellan Robotic System

NCT01984437 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 348

Last updated 2018-03-01

No results posted yet for this study

Summary

The purpose of the registry is to gather both retrospective and prospective case data on the use of the commercially available Magellan Robotic System and Magellan Robotic Catheters in accordance with the approved intended use. For prospective cases, follow-up patient data will be collected at 14 days (± 5 days) post procedure to assess treatment success, primary patency of intended targeted vessel region, and adverse events.

The data will be analyzed for medical education, societal presentation, and/or publication by the investigators.

Over the next 2+ years, physicians who meet the selection criteria will be invited to participate in the registry.

Conditions

  • Peripheral Vascular Disease

Sponsors & Collaborators

  • Hansen Medical

    lead INDUSTRY

Principal Investigators

  • Jean Bismuth, MD · The Methodist Hospital Research Institute

  • Brenda Cayme, RN, BSN · Hansen Medical, Inc.

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-11-30
Primary Completion
2016-08-31
Completion
2016-08-31

Countries

  • United States
  • France
  • Germany

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 NCT01984437 on ClinicalTrials.gov