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NCT03793049: SEQUEL

Repeatability and Reproducibility of the CADence™System

Completed Last updated 10 July 2019
What this trial tests

trial testing CADence testing will be performed in Coronary Artery Disease in 79 participants. Completed in 26 June 2019.

Timeline
23 January 2019
Primary endpoint
26 June 2019
26 June 2019

Quick facts

Lead sponsorAUM Cardiovascular, Inc.
StatusCompleted
Study typeOBSERVATIONAL
Enrollment79
Start date23 January 2019
Primary completion26 June 2019
Estimated completion26 June 2019
Sites3 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

AUM Cardiovascular, Inc.

Who can join

22 and older, any sex, with Coronary Artery Disease. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study is designed as a prospective study to capture data for evaluating the repeatability and reproducibility of the CADence™ System. The study will be conducted at 3 different study sites using 6 CADence™ systems. Each subject will be tested 4 separate times by 2 different operators at each site and will be tested at all 3 site locations in order to accomplish this evaluation. The study will enroll a total of at least 24 CADence positive patients and at least 24 CADence negative patients.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Coronary Artery Disease

Currently open trials in the same condition.

Other AUM Cardiovascular, Inc. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03793049.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing