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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03018158
Other study ID # EC 15-019
Secondary ID
Status Completed
Phase N/A
First received December 28, 2016
Last updated April 9, 2018
Start date December 2016
Est. completion date March 2018

Study information

Verified date April 2018
Source Nihon University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The objective of this study was to compare level of artifact while tongue at rest and in motion of dentulous subjects.


Description:

The magnetic resonance imaging (MRI) is useful to diagnose soft tissue morphology, especially to detect cancer and disk displacement with temporomandibular disorders. The prevalence of tongue cancer may increase with ageing population. A clear MR image is indispensable for clinical diagnosis. However, tongue motion associated with the habitual or swallowing tongue movement may cause artifacts on MRI. This occurrence of motion artifact is speculated to be prominent with the patients without the occlusal support. The objective of this pilot study was to compare level of artifact while tongue at rest and in motion of dentulous subjects.


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date March 2018
Est. primary completion date March 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 100 Years
Eligibility Inclusion Criteria:

- dentulous

- edentulous classified Eichner' s classfication

Exclusion Criteria:

- involuntary motion occurs during imaging

- absolutely contraindicated or as a rule contraindicated of MRI examination

- subjects have ferromagnetic metals in the oral cavity

- subjects can not swallow naturally

Study Design


Related Conditions & MeSH terms


Intervention

Device:
denture wear.
MR Imaging was collected with or without denture wear.

Locations

Country Name City State
Japan Nihon University Hospital Matsudo Chiba

Sponsors (1)

Lead Sponsor Collaborator
Nihon University

Country where clinical trial is conducted

Japan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Luminance standard deviation value on MR image MR Imaging was collected with each condition.Through study completion, an average of 2 year
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