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Angiographic Comparison in an Observational Study of CADence (The AMBIENCE Study)

NCT02515825 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 101

Last updated 2021-04-08

Study results available
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Summary

This is a prospective, multi-center study to capture information on sensitivity and specificity of CADence using coronary angiogram as the gold standard, on subjects who are already scheduled for coronary angiography.

Conditions

Interventions

DEVICE

CADence

Sponsors & Collaborators

  • AUM Cardiovascular, Inc.

    lead INDUSTRY

Principal Investigators

  • Carmelo Panetta, MD · University of Minnesota

Eligibility

Min Age
41 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-05-31
Primary Completion
2016-06-30
Completion
2016-06-30
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

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 NCT02515825 on ClinicalTrials.gov