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Magnetic Resonance Imaging Study on Patients With Hemifacial Spasm (MRI-HFS)

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Xi'an Jiaotong University

Status

Enrolling

Conditions

Magnetic Resonance Imaging
Hemifacial Spasm

Treatments

Device: Scanning with magnetic resonance imaging

Study type

Observational

Funder types

Other

Identifiers

NCT04645277
XJTU1AF-CRF-2020-017

Details and patient eligibility

About

Up to now, multiplanar reconstruction (MPR) has been widely used to detect the neurovascular compressions (NVC) on the patients with hemifacial spasm (HFS). However, due to lack of stereoscopic vision, this traditional method sometimes can not meet the requirement on identifying the details of NVC, especially when the aberrant vessels turn out to be veins not arteries. The three dimensional analytic techniques, such as curved planar reconstruction (CPR) and magnetic resonance virtual endoscopy (MRVE), may be helpful to improve the sensitivity and specificity on the demonstration of NVC with stereo and dynamic views, so as to assist the design of the surgical plan.

Furthermore, the frequent finding of NVC on MRI studies of asymptomatic patients incited the creation of several strict criteria for the imaging diagnosis of NVC: the vessel must cross perpendicular to the long axis of the nerve, the nerve must be deviated or indented at the root entry zoon (REZ) by the vessel. Alternatively, morphological measurement of the nerve may correlate with the severity of facial spasm due to atrophy of the nerve in most cases of HFS, and is likely secondary to the micro-structural abnormalities, such as axonal loss, demyelination, collagen deposition, etc. In this study, cross-sectional area (CSA) and volume (V) of the cisternal facial nerve will be assessed to determine whether it can be a useful biomarker for predicting the degree of HFS.

Enrollment

60 estimated patients

Sex

All

Ages

20 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Primary HFS patients according to medical history and typical facial muscle spasms that are unilateral, involuntary, and had intermittent contractions innervated by the ipsilateral facial nerve. The patient has 1 year disease duration at least.

Exclusion criteria

  • Secondary causes of HFS, such as tumors or cysts compressing the facial nerve in the cerebellar pontine cistern; Precarious general health status; Percutaneous lesions or surgical treatments; Cardiac pacemaker or metal implants.

Trial design

60 participants in 2 patient groups

Patients with MRI using two dimensional reconstruction
Treatment:
Device: Scanning with magnetic resonance imaging
Patients with MRI using three dimensional reconstruction
Treatment:
Device: Scanning with magnetic resonance imaging

Trial contacts and locations

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Central trial contact

Yuan Wang, M.D.; Chenguang Guo, M.D.

Data sourced from clinicaltrials.gov

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