To evaluate the affect Oxtellar XR (Extended Release) has on neurology patients with trigeminal neuralgia (TN), and if it impacts their quality of life.
Oxcarbazepine has been used off-label for TN for many years, but has a twice daily dosing. With the once daily dosing it should theoretically help with patient adherence and possibly decrease side effects, which is common with extended release formulations. Specifically the investigators are looking at how well tolerated Oxtellar XR is, and if it has the same efficacy as standard treatments. It is a pilot study, so it will be difficult to gather data and have powerful outcomes, but this will give pilot data for future trials. Patients will be screened for inclusion and exclusion criteria and after will participate in 3 visits following the initial one. Various tests will be administered to measure treatment satisfaction and tolerability throughout the visits. The patients will not have to pay for any of the study visits or medications. A parking voucher will be provided as needed.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Oxtellar XR
Change in pain associated with trigeminal neuralgia (BPI)
Pain associated with trigeminal neuralgia as measured by the Brief Pain Inventory (BPI) facial.
Time frame: Weeks 2, 6, and 10 following screening
Change in pain associated with trigeminal neuralgia (VAS)
Pain associated with trigeminal neuralgia as measured by a Visiual Analog Scale (VAS).
Time frame: Weeks 2, 6, and 10 following screening
Change in Quality of Life
The Subjects Quality of life will be evaluated based on the their responses to the following endpoint: treatment satisfaction QOL questionnaire
Time frame: Weeks 2, 6, and 10 following screening
Change in Safety: Number of Attacks
The subjects Safety profile will be measured based upon the number of attacks experienced.
Time frame: Weeks 2, 6, and 10 following screening
Change in Safety: SF-12 Survey
The subjects Safety profile will be measured based upon completion of the SF-12 survey
Time frame: Weeks 2, 6, and 10 following screening
Change in Safety: Heart Rate
The subjects Safety profile will be measured based upon any noted changes in heart rate.
Time frame: Weeks 2, 6, and 10 following screening
Change in Safety: Blood Pressure
The subjects Safety profile will be measured based upon any noted changes in Blood pressure.
Time frame: Weeks 2, 6, and 10 following screening
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Change in Safety: CBC
The subjects Safety profile will be measured based upon a complete blood count (CBC).
Time frame: Weeks 2, 6, and 10 following screening
Change in Safety: CMP
The subjects Safety profile will be measured based upon a Comprehensive Metabolic Panel (CMP).
Time frame: Weeks 2, 6, and 10 following screening
Change in Treatment Satisfaction
Treatment satisfaction will be measured through the completion of the Treatment Satisfaction Questionnaire For Medication (TSQM).
Time frame: Weeks 2, 6, and 10 following screening
Change in Tolerability: Number of Attacks
Change in Tolerability will be measured by the number of attacks.
Time frame: Weeks 2, 6, and 10 following screening
Change in Tolerability: SF-12 Survey
Change in Tolerability will be measured by the completion of the SF-12 survey.
Time frame: Weeks 2, 6, and 10 following screening
Change in Tolerability: Vital Signs
Change in Tolerability will be measured by vital signs.
Time frame: Weeks 2, 6, and 10 following screening
Change in Tolerability: CBC
Change in Tolerability will be measured by a complete blood count (CBC).
Time frame: Weeks 2, 6, and 10 following screening
Change in Tolerability: CMP
Change in Tolerability will be measured by a comprehensive metabolic panel (CMP).
Time frame: Weeks 2, 6, and 10 following screening
Change in Tolerability: TSQM
Change in Tolerability will be measured by the completion of the Treatment Satisfaction Questionnaire For Medication (TSQM).
Time frame: Weeks 2, 6, and 10 following screening