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Clinical Trial Summary

To development of clinical assessment technique using multi-radiotracer positron emission tomography/magnetic resonance (PET/MR) in prostate cancer

- to establish the optimal imaging technique of PET/MR using multiple radioactive tracers for prostate cancer

- to establish the imaging biomarker using PET/MR for clinical assessment of prostate cancer and early detection of recurrent prostate cancer


Clinical Trial Description

To establish the optimal imaging technique of PET/MR using multiple radioactive tracers for prostate cancer

- Recruiting 30 patients with prostate cancer ahead to radical prostatectomy

- PET/MR using 18F-choline with dedicated prostate MRI in all patients

- PET/MR using 18fluoride(F)-fluorodeoxyglucose(FDG)in all patients after 2-7 days

- PET/CT using 18F-FDG in all patient immediate after 18F-FDG PET/MR

- outcome assessment: comparison of scan time, image quality, tumor detection rate, standardized uptake values of lesions

- establishing optimal imaging technique for prostate PET/MR

To establish the imaging biomarker using PET/MR for clinical assessment of prostate cancer

- comparison of findings on PET/MR, MRI and PET/CT with pathological mapping after radical prostatectomy

- outcome assessment: accuracy of PET/MR for localization and staging of prostate cancer compared with MRI only and PET/CT only

To establish the imaging biomarker using PET/MR for early detection of recurrent prostate cancer

- Recruiting 15 patients with recurrent prostate cancer treated by surgery, hormone, or radiation therapy

- Recruiting 15 patients with treated prostate cancer without recurrence

- PET/MR using 18F-choline with dedicated prostate MRI in all patients

- PET/MR using 18F-FDG in all patients after 2-7 days

- PET/CT using 18F-FDG in all patient immediate after 18F-FDG PET/MR

- comparison of findings on PET/MR, MRI, and PET/CT with clinical data in two patient groups with or without recurrent prostate cancer

- outcome assessment: accuracy of PET/MR for early detection and localization of recurrent prostate cancer compared with MRI only and PET/CT only ;


Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic


Related Conditions & MeSH terms


NCT number NCT01938339
Study type Interventional
Source Seoul National University Hospital
Contact Jeong Yeon Cho, MD
Phone 82-2-2072-3074
Email radjycho@snu.ac.kr
Status Recruiting
Phase N/A
Start date May 2012
Completion date December 2014

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