The Role of a Device to Evaluate the Neuromuscular Function in Assessing Muscle in Facial Paralysis Patients

Launched by UNIVERSITAIR ZIEKENHUIS BRUSSEL · Jun 30, 2015

Keywords

ClinConnect Summary

Facial paralysis has significant aesthetic, functional and psycho-social morbidity. The diagnosis and monitoring of neuromuscular recovery is limited to clinical examination, electromyography (EMG) and electroneurography (ENoG). EMG and ENoG is invasive for the patient and has practical and cost disadvantages. The MyotonPRO is a handheld device, which is pain-free and quick to use. Therefore this research is assessing MyotonPRO technology for this clinical application and may be effective at evaluating rehabilitative and surgical interventions. Phase 1 - Variation of measurements Phase 2 - ...

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • 1. unilateral peripheral facial nerve palsy
• • 2. Mental capacity to give consent
• • 3. The patient is able to sit independently
• Exclusion Criteria:
• • 1. Adults who have undertaken strenuous exercise within the last twenty-four hours
• • 2. Adults taking prescription medication with a known effect on the mechanical properties of muscle (e.g. benzodiazepines) or receiving antispasmodic medications (e.g. botulinum A toxin)
• • 3. Adults with poor mobility (unable to lie prone).
• • 4. Adults with a body mass index (BMI) \>30 kg/m2 . Muscle measurements may be inaccurate with excessive subcutaneous tissue