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OpenTrials
Completed

NCT Number: NCT02891889

Description of the Appearance of Brown Fat in Scanner

The aim of this study is to investigate aspects of brown fat in scanner with injection via the PET-CT study.

Completed

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

CHRU de Brest

Brest, 29609, France

About this study

Brown fat is metabolically active adipose tissue. It can be responsible in PET-CT of a fixation of 18-FDG and a look of pseudo-infiltration of fat. These aspects can be sources of false positives. The objective here is to gain a better knowledge of the scanner in areas of brown fat.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Consecutive patients since June 2014, who underwent a thoraco-abdominopelvic PET-CT examination with 18F-FDG in the University Hospital of Brest, in a clinical setting which warranted.
  • Major Patients
  • No opposition formalized

Exclusion criteria

  • Refusal of participation

Treatment and study plan

Primary outcomes

  1. Density value

    Time frame: 1 year

    measured by CT and expressed in Hounsfield Units

Secondary outcomes

  1. Standard Uptake Values (SUV) adipose tissue "white" and "brown".

    Time frame: 1 year

    SUV maximum and average

Sponsors and collaborators

Lead sponsor

University Hospital, Brest

Other

Registry information

Acronym: BAT

Important dates

Study start
2015
Primary completion
2015
Study completion
2015
First posted
Sep 8, 2016
Registry last updated
Sep 8, 2016

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.