HeRO Vascular Access Device Post Market Procedural Survey Protocol

NCT00889291 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 77

Last updated 2017-08-08

No results posted yet for this study

Summary

Post market observational survey of a vascular access device for access-challenged patients. Data collection efforts focused on patient medical and access history and implant procedure results.

Conditions

Sponsors & Collaborators

  • Merit Medical Systems, Inc.

    lead INDUSTRY

Principal Investigators

  • Marc Glickman, MD · Sentara Heart Hospital, Norfolk, VA

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-12-31
Primary Completion
2009-01-31
Completion
2009-01-31

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Entities

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 NCT00889291 on ClinicalTrials.gov