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MRI of the Liver With Eovist

Dynamic Contrast Evaluation of the Liver Using Gadoxetate Disodium (Eovist®) for Hepatocellular Carcinoma (HCC)

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01215838
Enrollment
4
Registered
2010-10-07
Start date
2010-08-31
Completion date
2012-01-31
Last updated
2013-10-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hepatocellular Carcinoma

Keywords

HCC, hepatocellular carcinoma, Eovist, MR, MRI, magnetic resonance

Brief summary

The purpose of this study is to determine if a new magnetic resonance (MR) protocol is better at diagnosing liver lesions.

Detailed description

Hepatocellular carcinoma (HCC), a form of liver cancer, is the seventh most common cause of cancer mortality in the US. The incidence rate of HCC is increasing along with the incidence of Hepatitis B and C which are known to promote HCC. Patients have a better prognosis (survival outlook) if HCC is found and treated at an early stage. MRI is the best imaging modality for diagnosing HCC. This study will compare standard MRIs and MRIs performed with a newly developed MR protocol to determine if it is possible to more confidently diagnose HCC.

Interventions

None listed

Sponsors

Bayer Healthcare Pharmaceuticals, Inc./Bayer Schering Pharma
CollaboratorINDUSTRY
University of Washington
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* known hepatocellular carcinoma * undergoing MRI of the liver

Exclusion criteria

* Contraindication to MRI with IV contrast

Design outcomes

Primary

MeasureTime frame
Accuracy of a new MR protocol in diagnosing HCC and other liver lesions.One day: participants will have one MRI of the liver.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026