Actively Recruiting
FArial NErf MRI in the Preoperative Assessment of PArotide Tumors
Led by Fondation Ophtalmologique Adolphe de Rothschild · Updated on 2026-01-05
88
Participants Needed
1
Research Sites
330 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
1. st visit: Inclusion, 3Tesla injected parotid MRI performed as part of routine care for characterization, to which two specific high resolution sequences will be added. Evaluation of the exact position of the parotid tumor relative to the trunk of the facial nerve and its first branches, classification into two categories: on contact (≤ 5 mm) or at a distance (\> 5 mm). 2. nd visit: Surgical intervention of the parotid tumor. The surgeon will specify the same data as that collected by the radiologists after the MRI. 3. rd visit: Post-operative consultation in the week following the intervention. The surgeon will look for the occurrence of post-operative facial paralysis.
CONDITIONS
Official Title
FArial NErf MRI in the Preoperative Assessment of PArotide Tumors
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient over 18 years old
- Candidate for first line surgery for a parotid tumor
- Parotid tumor located near the trunk of the facial nerve or its first branches based on clinical exam and imaging
- Affiliate or beneficiary of a social security scheme
- Written consent to participate in the study
You will not qualify if you...
- Personal history of surgery on the same side parotid gland
- Absolute or relative contraindication to MRI
- Known allergy to gadolinium contrast media
- Pre or post operative period of a liver transplant
- Patient under legal protection measures
- Pregnant or lactating woman
- Previous preoperative MRI for the current parotid lesion that was complete, well conducted, and interpretable
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Fondation A De Rothschild
Paris, PARIS, France, 75019
Actively Recruiting
Research Team
A
Amelie YAVCHITZ
CONTACT
A
Adrien COLLIN
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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