MRI Scan and Intra-labyrinthine Schwannoma

Sponsor
University Hospital, Strasbourg, France (Other)
Overall Status
Unknown status
CT.gov ID
NCT03580850
Collaborator
(none)
30
1
12
2.5

Study Details

Study Description

Brief Summary

Evaluate the interest of gadolinium for the positive and topographic diagnosis of intra-labyrinthine schwannoma, comparing T1 sequence acquired after gadolinium injection to a sequence of fast imaging type employing steady state acquisition (FIESTA-C)

Condition or Disease Intervention/Treatment Phase
  • Other: No intervention in this restrospective study

Study Design

Study Type:
Observational
Anticipated Enrollment :
30 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
INTEREST OF INTRAVENOUS INJECTION OF GADOLINIUM IN EXPLORATION INTRA-LABYRINTHINE SCHWANNOMA IN MRI 3 TESLAS
Actual Study Start Date :
Feb 2, 2018
Anticipated Primary Completion Date :
Feb 1, 2019
Anticipated Study Completion Date :
Feb 1, 2019

Outcome Measures

Primary Outcome Measures

  1. Presence or absence of intra labyrinthine vestibular nerve tumor using T2 FIESTA alone [1 hour after the realization of the MRI]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Age 18-80 years

  • Have intra-labyrinthine schwannoma

  • Have benefited from an MRI with gadolinium injection on the MRI 3T with interpretable sequences of good quality

  • Subject giving their consent for their participation

  • Subjects who benefited, between 2009 and 2016, from an MRI of the external auditory canals, with gadolinous product injection and on the 3 Tesla MRI, in which a diagnosis of intra labyrinthine schwannoma was made

Exclusion Criteria:
  • Refusal to participate in the study

Contacts and Locations

Locations

Site City State Country Postal Code
1 Service Imagerie 1 Strasbourg France 67098

Sponsors and Collaborators

  • University Hospital, Strasbourg, France

Investigators

  • Study Director: Francis VEILLON, MD, PhD, University Hospital, Strasbourg, France

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University Hospital, Strasbourg, France
ClinicalTrials.gov Identifier:
NCT03580850
Other Study ID Numbers:
  • 6809
First Posted:
Jul 9, 2018
Last Update Posted:
Jul 13, 2018
Last Verified:
Feb 1, 2018
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
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
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 13, 2018