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Evaluation of Treatment Response With Integrated MRI/PET in Patients With Hepatocellular Carcinoma

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National Taiwan University

Status

Unknown

Conditions

Hepatocellular Carcinoma

Treatments

Device: The imaging biomarkers determined by MR-PET

Study type

Observational

Funder types

Other

Identifiers

NCT02550613
201401081MIND

Details and patient eligibility

About

The purpose of this study is to explore the ability of integrated MRI/PET to detect and evaluate treatment outcome in HCC patients.

Full description

This study using 18F-FDG PET and functional MRI (DCE-MRI, Diffusion-weighted MRI, MR spectroscopy).

Enrollment

100 estimated patients

Sex

All

Ages

20 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Prior Informed Consent Form
  2. At least one measurable tumor, according to RECIST version 1.1.
  3. Age > 20 years.
  4. ECOG performance status 0 or 1.
  5. Life expectancy > 3 months.
  6. Confirmed Diagnosis of HCC
  7. Adequate renal function (Serum creatinine ≦ 1.5 x upper limit of normal).

Exclusion criteria

  1. Age <20 years old
  2. Pregnancy
  3. Contraindication for MRI: claustrophobia or MR non-compatible devices
  4. Contraindication for MR contrast medium: severe adverse reaction or impaired renal function (Cre > 2.0)
  5. History of other malignancy

Trial contacts and locations

1

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Central trial contact

Ting-Fang Shih, MD

Data sourced from clinicaltrials.gov

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