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Completed

NCT Number: NCT02999490

18F-FDG PET/CT in Diagnostic Patients of Disorder of Consciousness

Clinical examinations are difficult to discriminate between vegetative state and minimally conscious state. the diagnostic and prognostic usefulness of neuroimaging methods has not been established in a clinical setting. we will do a forward study of PET imaging in disorders of consciousness patients, and validate with clinical assessments with the coma recovery Scale-Revised(CRS-R).

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Key information

Age range

10 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

The PET/CT Centre Guangzhou General Hospital of Guangzhou Military Command

Guangzhou, Guangdong, 510000, China

About this study

Every patient need to be conducted the PET/CT scanning two times.The first time is resting state.The second time is stimulated state by watching a vedio.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Clinical diagnosis of disorder of consciousness

Exclusion criteria

-

Treatment and study plan

18F-FDG

Radiation

18F-FDG is positron emission tomography imaging agent which is already widely used in PET/CT examination.

Primary outcomes

  1. standardized uptake value

    Time frame: 60 mins after injecting 18F-FDG

Sponsors and collaborators

Lead sponsor

Guangzhou General Hospital of Guangzhou Military Command

Other

Registry information

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Dec 21, 2016
Registry last updated
Apr 20, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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