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User Evaluation Study of SyncVision System With Software v4.X

NCT02915991 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 35

Last updated 2018-05-14

No results posted yet for this study

Summary

This is a prospective, single-arm, unblinded, case observation study evaluating a commercially released 'Conformité Européenne' (CE)-mark co-registration software system along-side of a commercially- released CE-mark coronary physiology and X-ray system during routine clinical workflow. The purpose of this study is to collect Professional user feedback regarding clinical utility of the SyncVision 4.X system.

Conditions

Sponsors & Collaborators

  • Volcano Corporation

    lead INDUSTRY

Principal Investigators

  • Aaron Frimerman, Professor · The medical research and development fund for health services Hillel Yafe

  • Ariel Roguin, Professor · Rambam Healthcare Campus

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-11-30
Primary Completion
2017-08-31
Completion
2017-08-31

Countries

  • Israel

Study Locations

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Entities

Diseases

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 NCT02915991 on ClinicalTrials.gov