MRI With Gadoxetate Disodium in Measuring Tumors in Patients With Liver Cancer
Completed · Phase 1
Conditions studied: Adult Hepatocellular Carcinoma, Advanced Adult Hepatocellular Carcinoma, BCLC Stage 0 Adult Hepatocellular Carcinoma, BCLC Stage A Adult Hepatocellular Carcinoma, BCLC Stage B Adult Hepatocellular Carcinoma, BCLC Stage C Adult Hepatocellular Carcinoma, BCLC Stage D Adult Hepatocellular Carcinoma, Localized Non-Resectable Adult Liver Carcinoma, Localized Resectable Adult Liver Carcinoma
In brief
This pilot clinical trial studies magnetic resonance imaging (MRI) with gadoxetate disodium in measuring tumors in patients with liver cancer. Diagnostic procedures, such as MRI with gadoxetate disodium, may help find and diagnose liver cancer and find out how far the disease has spread. It is not yet known whether MRI with gadoxetate disodium provides a more precise measurement of liver tumors than standard computed tomography (CT).
Key facts
- Study ID
- NCT02578602
- Run by
- University of Southern California
- People needed
- 26
- Starts
- 2010-10-01
- Expected to finish
- 2015-06-01
- Last updated by the study team
- 2015-10-19
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- CT features suggestive of HCC, including those features which have been described herein; they are also enumerated below:
- For an arterially-enhancing lesion greater than or equal to 1 cm, but under 2 cm, all of the following criteria must be met:
- Imaging features of a mass
- Wash-out on later phases of contrast administration
- At least 1 cm or more growth
- For an arterially-enhancing lesion greater than or equal to 2 cm, two of the following criteria must be met:
- Imaging features of a mass
- Wash-out on later phases of contrast administration
- At least 1 cm or more growth
- All enhancing lesions with expansile, solid, enhancing tumor within vascular structures will be included, including the main portal vein, the main right and main left portal veins, the inferior vena cava (IVC), and the main hepatic veins
- No prior history of treatment of liver lesions
- Able to provide written and verbal informed consent
- Able to tolerate a complete abdominal MR examination, within 3 weeks of CT
You may not qualify if…
- Unable to provide written and verbal informed consent
- Unable to undergo MRI due to intraocular metallic foreign body, pacemaker, or other contraindications including objects in the body which are deemed to be unsafe or notable to be assessed, or unable to undergo MRI within 3 weeks of CT
- Pregnancy
- Severe renal insufficiency as defined by an estimated glomerular filtration rate of less than 30 cc/minute
- Severe liver disease as defined by Childs class C cirrhosis
- History of a previous reaction to contrast media
- History of bronchial asthma
- History of allergic disorders
- Acute renal insufficiency of any severity due to the hepato-renal syndrome or in the perioperative liver transplantation period
Where it is running
- USC / Norris Comprehensive Cancer Center — Los Angeles, California, United States
Full record on ClinicalTrials.gov
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