Patient Characteristics in Daily Radiological Practice of Gadovist® Application (PATRON)

Bayer3,711 enrolled

Overview

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).

Study Type

OBSERVATIONAL

Enrollment

3,711

Conditions

Epidemiologic Factors

Interventions

Gadobutrol (Gadovist, BAY86-4875)BIOLOGICAL

Patients with indication for a MRT or MR-Angiography and for whom the radiologist has decided to use the contrast medium gadobutrol

Eligibility

Sex: ALLMin age: 7 Years

Medical Language ↔ Plain English

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.

Locations (1)

Unnamed facility

Many Locations, Germany

Outcomes

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

Data from ClinicalTrials.gov

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