Lumason® Infusion vs. Bolus Administrations

Status Not yet recruiting

Clinical Trial Summary

A phase III study designed as a randomized, within-patient comparison of continuous infusion of diluted Lumason® versus the bolus administration of undiluted Lumason® for degree of LVO and assessment of LV EBD (co-primary endpoints).

Clinical Trial Description

This is a phase III study designed as a randomized, within-patient comparison of continuous infusion of diluted Lumason® versus the bolus administration of undiluted Lumason® for degree of LVO and assessment of LV EBD (co-primary endpoints). The study will enroll patients with suboptimal LV EBD defined as ≥2 adjacent segments in any apical view that cannot be visualized at pre-contrast echocardiogram. ;

Study Design

Related Conditions & MeSH terms

Heart Diseases

Clinical Trial Details

NCT number	NCT06400004
Study type	Interventional
Source	Bracco Diagnostics, Inc
Contact	Rushil Sankpal
Phone	609-514-2267
Email	rushil.sankpal@diag.bracco.com
Status	Not yet recruiting
Phase	Phase 3
Start date	April 30, 2024
Completion date	December 31, 2024

View Details

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