Status
Conditions
Treatments
About
This study aims to increase the understanding of the pathophysiology of trigeminal neuralgia by investigating the potential association between blink reflex abnormalities and phenotypical traits e.g. clinical characteristics and neuroimaging findings.
Full description
We hypothesize:
Patients with classical trigeminal neuralgia have a prolonged latency and reduced amplitudes of the blink-reflex on the pain side compared to patients with idiopathic TN
The latency and amplitudes of the blink-reflex is normal in patients with idiopathic trigeminal neuralgia
Patients with concomitant persistent pain have a prolonged latency and reduced amplitudes of the blink reflex on the pain side compared to patients with pure paroxysmal TN
More men than women have a prolonged latency and reduced amplitudes of the blink reflex
Patients with neurovascular contact with morphological changes have prolonged latency and reduced amplitudes of the blink reflex compared to patients with simple neurovascular contact
Patients with secondary TN have prolonged latency and reduced amplitudes of the blink reflex compared to patients with simple neurovascular contact
Patients with neurovascular contact with morphological changes have prolonged latency and reduced amplitudes of the blink reflex on the pain side compared to the non-pain side
Study population
All patients with the diagnosis of primary or secondary trigeminal neuralgia, seen in the outpatient clinic at the Danish Headache Center will be screened for eligibility to participate the study. Clinical routine is not influenced by participation in this observational study. Patients will be offered the same treatment as patients not participating.
Setting
All patients with classic, idiopathic and symptomatic TN who have an appointment with a physician at the outpatient clinic at the Danish Headache Center as part of their work-up will, when they arrive at the center for their appointment, be asked if they want to participate in the study. The patients will be asked consecutively and there will be no prior recruitment of the patients. See recruitment below section 6.1. The study will not influence decisions regarding treatment of TN for the patients included in this protocol. Patients will be treated at the discretion of their own physician and the assessments listed below, are an integrated part of the clinical work-up and follow-up.
Assessments
Standardised data obtained from the medical chart
The following data will be obtained and registered from the medical chart of each patient that is included in the study:
Gender, date of birth, family history of TN or other facial pain
Duration and localization of TN, use of and response to previous medical treatments
Severity of pain at the time of examination - using Verbal Numerical Rating Scale (VNRS)
Location and trigger factors for TN
Previous neurosurgical treatment for TN
Additional concomitant diseases and medication
Type and dosage of TN related medication, if any
The result of the neurological exam.
Short interview on the examination day
On the day of the blink reflex examination, each patient will be asked by a trained biomedical laboratory scientist, nurse or medical student about the following:
Then the number of paroxysms
The current level of pain (VNRS)
The current dosage of TN medicine, will be on the day of neurophysiological assessments.
The trained personnel will not ask about the side of pain and will not know the result of the MRI evaluation, so they are blinded in terms of side of pain and what type of TN patient they investigate.
Neuroradiological assessment
The 3.0 Tesla MRI, performed according to a special TN protocol will be evaluated by a neuroradiologist, blinded for pain side. The neuro imaging data will be taken from the patient electronic journal. The following data will be registered:
Degree (no contact, simple contact, displacement/compression or atrophy of the nerve), location and type (arterial, venous or mixed) of NVC
Neurophysiological assessment (blink-reflex)
Electromyographic Recording:
We want to record signals from both eyes (see image). Channel 1: left eye. Channel 2: right eye
After connecting the cables to Channels 1 and 2 we can connect the electrodes to the black and red terminal wires: Black cable à active electrode: placed on the midline of the lower eyelid (orbicularis oculi muscles). Red cable à reference electrode: lateral to the eye (where the bone is superficial) We need one Green cable àground electrode: forehead or shoulder.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
Age 18 years or older
Must be able to give Signed Informed Consent prior to study entry. Appendix X
Must fulfill the ICHD-3 diagnostic criteria1 for classical, idiopathic or secondary TN.
Has had a 3.0 Tesla MRI according to the trigeminal neuralgia protocol, maximum 2 years before or after the assessment of the blink-reflex.
Has had a semi-structured interview and neurological examination by the independent assessors, maximum 2 years before or after the assessment of the blink-reflex.
Exclusion criteria
If the patient is not able to give informed consent due to mental challenges
Previous neurosurgical treatment (microvascular decompression and/or ablative procedures) for trigeminal neuralgia
Bilateral trigeminal neuralgia
Symptomatic trigeminal neuralgia
Findings of sensory abnormalities detected at clinical neurological examination
Loading...
Data sourced from clinicaltrials.gov
Clinical trials
Research sites
Resources
Legal