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Clinical Trial Summary

The aim of this study is to evaluate the potential and feasibility of 18F-metafluorobenzylguanidine (18F-MFBG) positron emission tomography (PET) in patients with neural crest and neuroendocrine tumors.


Clinical Trial Description

Ten neural crest tumor or neuroendocrine tumor (NET) patients, with a routine clinical 123I-metaiodobenzylguanidine (123I-MIBG imaging) (planar + single photon emission tomography (SPECT)) performed in the previous six months or scheduled within three months, will undergo a dynamic PET scan for the first 30 minutes, followed by 3 static whole-body PET/CTs up to three hours post injection for a pharmacokinetics study and efficacy assessment of 18F-MFBG in humans. Furthermore, a comparison with 123I-MIBG imaging will be performed. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04258592
Study type Interventional
Source Universitaire Ziekenhuizen Leuven
Contact
Status Terminated
Phase Phase 1
Start date February 7, 2020
Completion date July 7, 2022

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