Viewing Study NCT00156845



Ignite Creation Date: 2024-05-05 @ 11:52 AM
Last Modification Date: 2024-10-26 @ 9:15 AM
Study NCT ID: NCT00156845
Status: COMPLETED
Last Update Posted: 2006-07-14
First Post: 2005-09-08

Brief Title: Phase 3 Safety and Imaging Study of AI-700 in Patients With Suspected Coronary Artery Disease Undergoing Coronary Angiography
Sponsor: Acusphere
Organization: Acusphere

Study Overview

Official Title: A Phase 3 International Multicenter Open-Label Dual-Injection Echocardiographic Imaging and Safety Study in Patients With Suspected Ischemic Heart Disease Undergoing Diagnostic Coronary Angiography Real-Time Assessment of Myocardial Perfusion With Echocardiography RAMP 2
Status: COMPLETED
Status Verified Date: 2006-07
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This study was designed to evaluate the ability of AI-700-enhanced rest-stress echocardiography to detect coronary artery disease CAD in patients with suspected ischemic heart disease who are indicated for coronary angiography
Detailed Description: Assessment of myocardial perfusion has been demonstrated to provide both diagnostic and prognostic value to patients with ischemic heart disease by allowing the clinician to assess the hemodynamic significance of coronary artery disease CAD The primary objective of the clinical development program for AI-700 is to demonstrate the safety and efficacy of AI-700 as an intravenous ultrasound contrast agent in patients with suspected myocardial perfusion defects

The patient population is comprised of patients being evaluated for inducible ischemia and indicated for coronary angiography The primary study objective was to determine the accuracy sensitivity and specificity of AI-700-enhanced echocardiographic imaging for detecting CAD using coronary angiographyleft ventriculography ANGIOLVG as the reference standard

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None