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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02903550
Other study ID # 2015-27
Secondary ID
Status Recruiting
Phase N/A
First received September 13, 2016
Last updated March 12, 2018
Start date August 2015
Est. completion date March 2018

Study information

Verified date March 2018
Source Assistance Publique Hopitaux De Marseille
Contact Arthur VAROQUAUX
Email arthur.varoquaux@ap-hm.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Cholesteatoma is a destructive and expanding pathologic condition consisting of keratin pearl arising from a squamous epithelium in the middle ear and/or mastoid process. Evolution consists in a destruction of the ossicles as well as their possible spread through the base of the skull into the brain. Surgical treatment is required to prevent infectious or functional complications. A recurrence after surgery occurs in approximately 10% of patients and rarely affects initial site. Surgical treatment is the only care option for recurrent cholesteatoma. Various locations such as surgical approach cavity, mastoid, hypotympanum are seen. Temporal bone CT is performed prior to surgery for added information on bone erosions especially of ossicules, tegmen tympani, facial nerve canal of internal ear. Due high anatomical resolution and complex anatomy, temporal bone CT is usually displayed with Magnetic Resonance Imaging (MRI) in operating room to help surgical guidance .

Imaging especially using MRI is the cornerstone for diagnosis in asymptomatic patients. Since 2006, non echo planar imaging (EPI) Diffusion weighted imaging (DWI) Magnetic resonance imaging (MRI) (sequences has shown high accuracy to depict recurrent cholesteatoma. If EPI sequences had a high rate of diffeomorphic atefacts whereas non EPI sequences using either HAlf-Fourier acquisition Single-shot Turbo spin-Echo (HASTE) or Fast-spin-echo demonstrates less magnetic susceptibility artifacts. Multimodality fusion between NonEPI-DWI-MRI and computerized tomography (CT) is a rational promising tool to rise the performance for cholesteatomas delineation. The performances of NonEPI-DWI-MRI in assessing lesion spread and volume are still unknown and needs further investigations. The aim of the study is to assess the DWI-MRI/CT fusion feasibility, reproducibility and the accuracy prior to surgery propectively compared to surgical findings.


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date March 2018
Est. primary completion date August 2017
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Adult woman or man who had surgery and suspicion of cholesteatoma recurrence

Exclusion Criteria:

- Chronic renal failure

- Contraindications to MRI

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Hôpital de La Timone - Assistance Publique Hôpitaux de Marseille Marseille Cedex 05

Sponsors (1)

Lead Sponsor Collaborator
Assistance Publique Hopitaux De Marseille

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Determination of the lesion on the scanner with the help of MRI, but without having merged both methods UP to 18 months
Primary Measure of the lesion volume in mm3 Up to 18 months
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