Viewing Study NCT01206257


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Study NCT ID: NCT01206257
Status: COMPLETED
Last Update Posted: 2013-06-11
First Post: 2010-09-20
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: The Safety and toleRability of UltraviSt in Patients Undergoing Cardiac CaTheterization (TRUST)
Sponsor: Bayer
Organization:

Study Overview

Official Title: This is an International, Prospective, Non-interventional Study, Company Sponsored, Multi-center Study. Patients Undergo Coronary Angiography or PCI Procedure With Ultravist. The Primary Objective is to Evaluate the Safety and Tolerability.
Status: COMPLETED
Status Verified Date: 2013-06
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: TRUST
Brief Summary: This study is to collect the information of Ultravist® in the patients indicated for the coronary angiography or PCI, like rate of ADR in patients, the dose for different indications, image quality to prove Ultravist the good safety and effectivity
Detailed Description: None

Study Oversight

Has Oversight DMC: False
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?:

Secondary ID Infos

Secondary ID Type Domain Link View
UV1010CN OTHER company internal View