Many Locations, Germany
NCT Number: NCT00874640
Patient Characteristics in Daily Radiological Practice of Gadovist® Application (PATRON)
To evaluate patient characteristics in the current daily radiological practice of Gadovist application. Special focus will be laid on the individual risk factors of patients, the indications for and the dose of Gadovist application.
Secondary objective is to prove the known safety profile (especially rare adverse events) of Gadovist and to collect data on handling problems with different application forms (one questionnaire per center).
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Notify MeKey information
Conditions
Age range
7 year and older
Sex eligibility
All sexes
Study type
Observational
Primary location
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- patients with indication for a MRT or MR-Angiography and for whom the radiologist has decided to use the contrast medium Gadovist
Exclusion criteria
- No exclusion criteria besides the contraindications for the use of Gadovist as mentioned in the German product information.
Treatment and study plan
Gadobutrol (Gadovist, BAY86-4875)
BiologicalPatients with indication for a MRT or MR-Angiography and for whom the radiologist has decided to use the contrast medium gadobutrol
Primary outcomes
-
Patient Profile
Time frame: At day of application
Secondary outcomes
-
Dosing of Gadovist in different indications
Time frame: At time of application
-
Adverse Events
Time frame: Throughout and after application
Sponsors and collaborators
Lead sponsor
Bayer
Industry
Registry information
Important dates
- Study start
- 2009
- Primary completion
- 2011
- Study completion
- 2011
- First posted
- Apr 2, 2009
- Registry last updated
- Feb 20, 2014
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.