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Clinical Trials/NCT01231282
NCT01231282
Completed
Not Applicable

Technique Optimization and Anatomy of the Human Body With Whole-body Diffusion-weighted MRI: Study With Healthy Volunteers

Universitaire Ziekenhuizen KU Leuven1 site in 1 country30 target enrollmentNovember 2010
ConditionsHealthy

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Healthy
Sponsor
Universitaire Ziekenhuizen KU Leuven
Enrollment
30
Locations
1
Primary Endpoint
normal aspect of human anatomy on WB-DWI images/ technique optimization
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

Whole body diffusion-weighted imaging is a functional magnetic resonance imaging technique that characterizes tissue by probing changes in water diffusion secondary to differences in the tissue microstructure. These changes in water diffusion result in differences in signal intensity on diffusion-weighted images that are quantified with the apparent diffusion coefficient (ADC). In malignant lesions, the extravascular extracellular space (EES) will be diminished, due to the increased number of cells. This will restrict water diffusion, identified by increased signal intensity (SI) on native diffusion-weighted images and low ADC. Contrary, in tissue with low cellularity, like benign lesions and treatment induced necrosis, the EES will be enlarged due to the lower density of cells, or in case of necrosis, the complete absence of cellular organization. This will facilitate water diffusion, leading to absent SI on native diffusion-weighted images and high ADC.

The purpose of this study is to image anatomy and lymph nodes in healthy volunteers with whole body diffusion-weighted imaging. This way maps of normal anatomy can be created on the whole body diffusion-weighted images which can be used as a reference in further studies with patients scanned with the same whole body diffusion-weighted imaging scan protocol.

A group of 30 healthy volunteers will receive a whole body diffusion-weighted imaging scan on a 3 Tesla T-MRI system.

A total scan session will take about 30 minutes. Contrast administration is not required and patients will not be exposed to radiation.

Registry
clinicaltrials.gov
Start Date
November 2010
End Date
April 2013
Last Updated
9 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • healthy volunteers

Exclusion Criteria

  • no severe illness in the past
  • no current infection/inflammation

Outcomes

Primary Outcomes

normal aspect of human anatomy on WB-DWI images/ technique optimization

Time Frame: up to 12 months

assessment after all the scans of the healthy volunteers are collected

Study Sites (1)

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