Study to Determine Safety and Dosage of OPTISON in Pediatric Participants

Transthoracic Echocardiography Clinical Trial

Official title:
A Phase 4, Open-Label, Non-Randomized, Multicenter Study to Evaluate Safety and Efficacy of Intravenous Administration of OPTISON™ for Contrast- Enhanced Echocardiography in Pediatric Patients

Status Completed

Clinical Trial Summary

Study to determine the safety and appropriate dosage of OPTISON in pediatric participants since OPTISON has been tested in adult participants only during the clinical development

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03740997
Study type	Interventional
Source	GE Healthcare
Contact
Status	Completed
Phase	Phase 4
Start date	December 1, 2020
Completion date	March 30, 2023

View Details

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