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NCT06986733: SMART-CCTA-1

Study of Management Alterations Resulting From CaRi-Heart® Technology in Patients Undergoing Coronary Computed Tomography Angiography (CCTA) for the Evaluation of Coronary Artery Disease: A United States Based Multi-Centre Study (SMART-CCTA-1)

Not yet recruiting Last updated 23 May 2025
What this trial tests

trial in Cardiovascular Diseases in 300 participants. Not yet recruiting.

Timeline
1 June 2025
Primary endpoint
31 December 2025
31 December 2025

Quick facts

Lead sponsorCaristo Diagnostics Limited
StatusNot yet recruiting
Study typeOBSERVATIONAL
Enrollment300
Start date1 June 2025
Primary completion31 December 2025
Estimated completion31 December 2025

Conditions studied

Sponsor

Caristo Diagnostics Limited

Who can join

Adults 30 to 80, any sex, with Cardiovascular Diseases. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study is an assessment of the impact of CaRi-Heart® on the clinical management of patients across at least three centres in the USA. This study is an observational study, in which clinicians will be presented with a patient's CCTA scan results and relevant clinical details (such as blood test results and clinical risk factors) with the resulting clinical management recommendation recorded; they will then be presented with the results of the CaRi-Heart® analysis alongside any other relevant clinical details and any changes in clinical management recommendation will be recorded.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Cardiovascular Diseases

Currently open trials in the same condition.

Other Caristo Diagnostics Limited 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/NCT06986733.

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