Viewing Study NCT00783302



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Last Modification Date: 2024-10-26 @ 9:57 AM
Study NCT ID: NCT00783302
Status: COMPLETED
Last Update Posted: 2014-12-11
First Post: 2008-10-30

Brief Title: Study in Subjects Suspected of Having CAD Undergoing VISIPAQUE-enhanced CCTA as Part of Their Routine Medical Care
Sponsor: GE Healthcare
Organization: GE Healthcare

Study Overview

Official Title: A Prospective Multi-Center Registry Study for Clinical Outcome in Subjects Undergoing Coronary Computed Tomography Angiography CCTA Examination VISIPAQUE Registry Study
Status: COMPLETED
Status Verified Date: 2014-12
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: To assess prognostic value of CCTA examination in subjects who undergo CCTA as part of their medical care when compared to a standard of truth ie subject outcomes during each follow-up period
Detailed Description: None

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