About this trial
70 stroke patients with central facial paralysis will be included and their demographic data will be questioned and facial nerve thickness, depressor labi inferior, depressor anguli oris, buccinator and risorius muscles will be evaluated.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Diagnosis of stroke and presence of unilateral central facial paralysis,
Agreeing to participate in the study,
Cognitive competence to understand the test instructions,
Presence of communication skills to respond to the test instructions.
Disqualifiers
Presence of previous facial paralysis or a neurological disease other than stroke that will cause central paralysis,
bilateral involvement
illiteracy, refusal to participate in the study,
jaw joint problem,
Trial population
70 stroke patients with central facial paralysis who were included in the rehabilitation program at Istanbul Physical Therapy and Rehabilitation Training and Research Hospital will be included
Trial design
Case-only
Cross-sectional
Treatments tested in this trial
ultrasonographic evaluation
Diagnostic testfacial nerve thickness (right/left), depressor labi inferior, depressor anguli oris, buccinator and risorius muscles will be evaluated.
Treatment groups
Trial outcomes
Primary outcomes
facial nerve thickness
the thickness of the nerve will be measured by ultrasound
Secondary outcomes
depressor labi inferior
the thickness of the muscle will be measured by ultrasound
depressor anguli oris
the thickness of the muscle will be measured by ultrasound
Locations
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
This trial is not recruiting at the moment. You can still explore other options: