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Completed Phase 3 Interventional Results available

Gadobutrol Enhanced MRA of the Supra-aortic Vessels

ClinicalTrials.gov ID: NCT01344447

Public ClinicalTrials.gov record NCT01344447. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 12:48 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Multicenter, Open-label Study to Evaluate the Safety and Efficacy (by Blinded Reading) of Contrast-Enhanced Magnetic Resonance Angiography (MRA) After a Single Intravenous Injection of 0.1 mmol/kg Gadobutrol in Subjects With Known or Suspected Vascular Disease of the Supra-aortic Vessels

Study identification

NCT ID
NCT01344447
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Bayer
Industry
Enrollment
479 participants

Conditions and interventions

Interventions

  • Gadobutrol (Gadovist, BAY86-4875) Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 11, 2011
Primary completion
May 27, 2014
Completion
May 27, 2014
Last update posted
Jan 3, 2019

2011 – 2014

United States locations

U.S. sites
15
U.S. states
14
U.S. cities
15
Facility City State ZIP Site status
Not listed Tucson Arizona 85724
Not listed Jacksonville Florida 32209
Not listed Savannah Georgia 31406
Not listed Louisville Kentucky 40202
Not listed Baltimore Maryland 21201
Not listed Boston Massachusetts 02114
Not listed Ann Arbor Michigan 48109-0330
Not listed Jackson Mississippi 39216
Not listed Rochester New York 14642
Not listed The Bronx New York 10467
Not listed Philadelphia Pennsylvania 19104
Not listed Providence Rhode Island 02903
Not listed Memphis Tennessee 38104
Not listed Seattle Washington 98195
Not listed Madison Wisconsin 53792

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 41 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01344447, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 3, 2019 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01344447 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →