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Antineuralgic Effect of Lacosamide (Vimpat) in Trigeminal Neuralgia Patients

Antineuralgic Effect of Lacosamide (Vimpat) in Trigeminal Neuralgia Patients

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20210811002
Enrollment
48
Registered
2021-08-11
Start date
2021-03-08
Completion date
Unknown
Last updated
2026-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Trigeminal neuralgia (TN) is a rare neuropahic condition with symptoms as brief, abrupt onset electric shock-like pain in the area of trigeminal nerve innervation. Trigeminal neuralgia Neuropathic pain

Interventions

Placebo for control group,Lacosamide 200 mg/day ,Lacosamide 400 mg/day
Control group,Low dose group,High dose group

Sponsors

Neurosciences Research and Development Group, Khonkaen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Adult 2. Diagnosed as trigeminal neuralgia according to International Classification of Headache Disorder 3rd edition (ICHD-3) 3. Numeric rating scale of pain higher than 4 4. Never received any treatment or have not taken any drugs in last 4 weeks 5. Physical condition is categorized as American Society of Anesthesiologist (ASA classification) 1 or 2 6. Can communicate in Thai

Exclusion criteria

Exclusion criteria: 1. History of microvascular decompression surgery without recurred symptom 2. Impaired physical condition or psychological problems 3. Pregnancy and lactation 4. History of suicide commitment 5. Impaired liver or kidney functions 6. History of experimental drug allergy 7. Unwilling to join the sudy 8. Could not come to follow up regularly

Design outcomes

Primary

MeasureTime frame
Pain intensity Baseline, 2weeks, 4 weeks and 8 weeks after numeric rating scale

Secondary

MeasureTime frame
Physical function Baseline, 2weeks, 4 weeks and 8 weeks after BPI-facial questionnaire,Emotional function Baseline, 2weeks, 4 weeks and 8 weeks after Thai Hospital anxiety and depression scales questionnaire,Adverse effects Baseline, 2weeks, 4 weeks and 8 weeks after Blood investigation (complete blood count, liver function test, creatinine, electrolytes),Pain quality Baseline, 2weeks, 4 weeks and 8 weeks after Neuropathic Pain Symptoms Inventory (NPSI)

Countries

Thailand

Contacts

Public ContactTeekayu Jorns

Khonkaen University

teepla@kku.ac.th66897982505

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Apr 4, 2026