RecruitingNCT05582915

Screening for Prognostic Biomarkers of Severe Bell's Palsy in Adults

Screening for Prognostic Biomarkers of Severe Bell's Palsy in Adults Using Proteomic Analysis by Quantitative Mass Spectroscopy


Sponsor

University Hospital, Montpellier

Enrollment

130 participants

Start Date

Jan 3, 2023

Study Type

OBSERVATIONAL

Conditions

Summary

Bell's palsy (idiopathic peripheral facial palsy) is the most common cause of facial palsy, which is related to the inflammation of the facial nerve, possibly induced by herpesvirus reactivation. Its first-line treatment comprises corticosteroids, antiviral therapy and physiotherapy. In most severe cases (grade IV to VI on House-Brackmann scale), facial motricity may remain altered or develop synkinesis or post-paralytic spasm, thus tremendously affecting quality of life. To avoid potential complications, surgical facial nerve decompression could be proposed. To date, however, there are no means to predict if Bell's palsy will evolve with any complications or if the patient will recover entirely. Thus, the invasive facial nerve decompression is equally proposed to subjects who will develop the consequences as well as to subjects able to restore without surgical treatment. This study proposes to search for prognostic blood biomarkers related to the Bell's palsy recovery pattern. Adult patients with severe Bell's palsy will be proposed to have a blood sampling for proteomic analysis in the early stage of the disease. Then 125 biomarkers on a Peptiquant™ kit will be analysed by mass spectrometry, and prognostic biomarkers will be selected regarding to the clinical recovery of Bell's palsy


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

Bell's palsy is a sudden weakness or paralysis of one side of the face. Most people recover fully, but some do not. This study looks for biological markers (biomarkers) in the blood and brain that can predict who will have a harder time recovering, so that doctors can identify and better support those patients early. You may be eligible if: - You have severe Bell's palsy (rated House-Brackmann grade IV or higher) - Your symptoms developed between 5 and 15 days before your first study visit - You are 18 years or older You may NOT be eligible if: - Your facial palsy has a known cause other than Bell's palsy (such as diabetes, Lyme disease, herpes zoster, a tumor, or a head injury) - You are on anti-inflammatory or immunosuppressive treatment - You have a contraindication to MRI - You are pregnant or breastfeeding - You cannot understand or consent to the study - You are participating in another interventional study Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DIAGNOSTIC_TESTBlood sampling

4 ml of blood will be collected into EDTA tube for proteomic analysis at visit 0 and visit 1


Locations(1)

CHU Montpellier

Montpellier, France

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NCT05582915


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