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

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

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02550613
Enrollment
100
Registered
2015-09-15
Start date
2014-05-31
Completion date
2018-04-30
Last updated
2017-05-16

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

Conditions

Hepatocellular Carcinoma

Keywords

MR/PET, hepatocellular carcinoma, HCC

Brief summary

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

Detailed description

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

Interventions

The purpose of this study is to explore the ability of integrated MRI/PET to detect and evaluate treatment outcome in HCC patients. This study using 18F-FDG PET and functional MRI (DCE-MRI, Diffusion-weighted MRI, MR spectroscopy).

Sponsors

National Taiwan University Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
20 Years to 90 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
The recurrence rate at 3 months after treatment3 months

Secondary

MeasureTime frame
The overall survival after treatment1 year

Countries

Taiwan

Contacts

Primary ContactTing-Fang Shih, MD
ttfshih@ntu.edu.tw+886-2-23123456

Outcome results

None listed

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