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Clinical Trial Summary

This is an open-label dynamic whole-body PET/CT (positron emission tomography/computed tomography) study for investigation of radiation dosimetry, plasma pharmacokinetics, biodistribution, safety and diagnostic performance of 18F-S16 in healthy volunteers and patients with neurodegenerative dementia.


Clinical Trial Description

For interests in clinical translation of 18F-S16, an open-label dynamic whole-body PET/CT study was designed to investigate safety and diagnostic performance of 18F-S16 in patients with neurodegenerative dementia. A single dose of nearly 370 MBq 18F-S16 will be intravenously injected into healthy volunteers and patients with neurodegenerative dementia. Visual and semiquantitative method will be used to assess the PET/CT images. Changes of blood pressure, pulse, respiration, temperature, routine blood and urine tests, serum alanine aminotransferase, albumin, and creatinine, and any adverse events will be collected from the subjects. Adverse events will also be observed in the subjects. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03620552
Study type Interventional
Source Oriental Neurosurgery Evidence-Based-Study Team
Contact Li Cai, MD
Phone 86-22-60362190
Email XCL242004@126.com
Status Recruiting
Phase Early Phase 1
Start date August 20, 2017
Completion date February 20, 2019