Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
4 participants
OBSERVATIONAL
2010-08-31
2012-01-31
Brief Summary
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Detailed Description
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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.
Conditions
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Keywords
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* undergoing MRI of the liver
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Bayer Healthcare Pharmaceuticals, Inc./Bayer Schering Pharma
INDUSTRY
University of Washington
OTHER
Responsible Party
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Principal Investigators
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Orpheus Kolokythas, MD
Role: PRINCIPAL_INVESTIGATOR
University of Washington
References
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Jemal A, Siegel R, Ward E, Murray T, Xu J, Smigal C, Thun MJ. Cancer statistics, 2006. CA Cancer J Clin. 2006 Mar-Apr;56(2):106-30. doi: 10.3322/canjclin.56.2.106.
Saito K, Kotake F, Ito N, Ozuki T, Mikami R, Abe K, Shimazaki Y. Gd-EOB-DTPA enhanced MRI for hepatocellular carcinoma: quantitative evaluation of tumor enhancement in hepatobiliary phase. Magn Reson Med Sci. 2005;4(1):1-9. doi: 10.2463/mrms.4.1.
Frericks BB, Loddenkemper C, Huppertz A, Valdeig S, Stroux A, Seja M, Wolf KJ, Albrecht T. Qualitative and quantitative evaluation of hepatocellular carcinoma and cirrhotic liver enhancement using Gd-EOB-DTPA. AJR Am J Roentgenol. 2009 Oct;193(4):1053-60. doi: 10.2214/AJR.08.1946.
Other Identifiers
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7160
Identifier Type: OTHER
Identifier Source: secondary_id
DI-2009-1
Identifier Type: -
Identifier Source: org_study_id