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3D Model of Posterior Membranous Labyrinth of the Inner Ear

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ClinicalTrials.gov Identifier: NCT03295929
Recruitment Status : Unknown
Verified September 2017 by University Hospital, Strasbourg, France.
Recruitment status was:  Recruiting
First Posted : September 28, 2017
Last Update Posted : February 27, 2018
Sponsor:
Information provided by (Responsible Party):
University Hospital, Strasbourg, France

Brief Summary:
The aim of this work is to create a three-dimensional (3D) finite element model (FEM) of the human posterior membranous labyrinth, based on in vivo inner ear magnetic resonance imaging (MRI). This model has a pedagogical interest, and can serve as a basis for reflection in cases of atypical benign paroxysmal positional vertigos. It can also serve for mechanical studies of vestibular physiology.

Condition or disease
Reconstruction of the Posterior Membranous Labyrinth

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Study Type : Observational
Estimated Enrollment : 1 participants
Observational Model: Other
Time Perspective: Retrospective
Official Title: 3D Finite Element Model of Posterior Membranous Labyrinth From in Vivo MRI of Human Temporal Bone
Actual Study Start Date : October 19, 2017
Estimated Primary Completion Date : September 2018
Estimated Study Completion Date : September 2018



Primary Outcome Measures :
  1. Measure of dimensions of the model to study the validity of the geometry [ Time Frame: Creation of 3D model: 1 month ]


Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Sampling Method:   Non-Probability Sample
Study Population
Adult who has performed an imaging of the inner ear
Criteria

Inclusion Criteria:

  • Patient aged 18 or over
  • Adult who has performed an imaging of the inner ear

Exclusion Criteria:

  • Refusal to participate in the study

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03295929


Contacts
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Contact: Anne CHARPIOT, MD, PhD 33 3 88 12 76 49 anne.charpiot@chru-strasbourg.fr
Contact: Hella VUONG, MD 33 6 50 66 82 23 hella.vuong@chru-strasbourg.fr

Locations
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France
Service D'Orl Et de Chirurgie Cervico-Faciale Recruiting
Strasbourg, France, 67091
Contact: Anne CHARPIOT, MD, PhD    33 3 88 12 76 49    anne.charpiot@chru-strasbourg.fr   
Contact: Hella VUONG, MD    33 6 50 66 82 23    hella.vuong@chru-strasbourg.fr   
Principal Investigator: Anne CHARPIOT, MD, PhD         
Sub-Investigator: Hella VUONG, MD         
Sponsors and Collaborators
University Hospital, Strasbourg, France

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Responsible Party: University Hospital, Strasbourg, France
ClinicalTrials.gov Identifier: NCT03295929     History of Changes
Other Study ID Numbers: 6815
First Posted: September 28, 2017    Key Record Dates
Last Update Posted: February 27, 2018
Last Verified: September 2017
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by University Hospital, Strasbourg, France:
3D model
Inner ear