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Last Updated: May 14, 2021

DrugPatentWatch Database Preview

CLINICAL TRIALS PROFILE FOR ULTRAVIST 150

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All Clinical Trials for Ultravist 150

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00244140 Ultravist: Safety and Efficacy in Computed Tomography of Head and Body Completed Bayer Phase 3 2005-10-01 This is a research study involving the use of a contrast agent called Ultravist Injection. Ultravist, the study drug, is used to improve the pictures obtained using computed tomography (CT). Ultravist acts like a dye to make CT pictures brighter and easier to read. In the case of this study, it will be injected into a vein in the patient's arm; from there, it travels through the blood stream and to the areas to be examined. CT scans will then be taken of the patient's head and/or body as ordered by his/her physician. Phase IIIb Study to Document the Safety and Efficacy of Ultravist 370 mg I/ml, When Administered Intravenously, in Volumes up to 162.2 ml, for Clinically Indicated Contrast Enhanced Computed Tomography (CECT) of the Head and/or Body
NCT00876083 PMS Study Ultravist-IMAGE, IoproMide (UltrAvist) to Gain Further Information on Tolerability and Safety in X-ray Examination Completed Bayer N/A 2008-03-01 The purpose of this study is to obtain data on the safety and efficacy of Ultravist application in usual daily use.The radiologist will administer the contrast medium to the patient as he/she would have done without the study. No other examinations will be performed than would have been done routinely.
NCT00926562 A Safety Comparison of Iopromide and Iodixanol in Renal Impaired Patients Completed Chinese PLA General Hospital Phase 4 2009-02-01 The investigators intend to find out which contrast agent has less kidney toxicity in renal impaired patients undergoing cardiac angiography or percutaneous coronary intervention (PCI).
NCT01206257 The Safety and toleRability of UltraviSt in Patients Undergoing Cardiac CaTheterization (TRUST) Completed Bayer N/A 2010-08-01 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
NCT01255722 Xenetix® 350: Comparative Assessment of Image Quality for Coronary CT Angiography Completed Guerbet Phase 4 2010-11-01 The purpose of this study is to demonstrate the (statistical) non-inferiority of iobitridol (Xenetix® 350) when compared to contrast agents with higher iodine concentrations, iopromide (Ultravist® 370) and iomeprol (Iomeron® 400) in terms of coronary CT scan evaluability (quality and interpretability of images).
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for Ultravist 150

Condition Name

Condition Name for Ultravist 150
Intervention Trials
Diagnostic Imaging 3
Kidney Failure, Chronic 2
Computed Tomography 1
Venous Thromboembolism 1
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Condition MeSH

Condition MeSH for Ultravist 150
Intervention Trials
Renal Insufficiency 2
Kidney Failure, Chronic 2
Venous Thromboembolism 1
Thromboembolism 1
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Clinical Trial Locations for Ultravist 150

Trials by Country

Trials by Country for Ultravist 150
Location Trials
China 23
United States 11
Korea, Republic of 3
Colombia 2
Switzerland 1
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Trials by US State

Trials by US State for Ultravist 150
Location Trials
Massachusetts 1
Maryland 1
Illinois 1
Georgia 1
Florida 1
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Clinical Trial Progress for Ultravist 150

Clinical Trial Phase

Clinical Trial Phase for Ultravist 150
Clinical Trial Phase Trials
Phase 4 5
Phase 3 1
Phase 2 1
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Clinical Trial Status

Clinical Trial Status for Ultravist 150
Clinical Trial Phase Trials
Completed 8
Unknown status 2
Not yet recruiting 1
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Clinical Trial Sponsors for Ultravist 150

Sponsor Name

Sponsor Name for Ultravist 150
Sponsor Trials
Bayer 5
Chinese PLA General Hospital 1
Duke Clinical Research Institute 1
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Sponsor Type

Sponsor Type for Ultravist 150
Sponsor Trials
Industry 7
Other 6
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