Health Condition 1: G448- Other specified headache syndromes
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients clinically diagnosed with TN according to the IHS Classification ICHD-3. 2. Both males and females. 3. Patients who have given informed consent for the study.
Exclusion criteria
Exclusion criteria: 1. Patients not willing to participate in the study. 2. Pregnant females. 3. Patients with abnormal CBC and liver function tests.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Reduction in pain intensity using McGill Pain Questionnaire.Timepoint: baseline and 3 months | — |
Secondary
| Measure | Time frame |
|---|---|
| Time taken for 50% pain reduction using VASTimepoint: twice weekly for initial 4 weeks , 1 month, 2 months and 3 months | — |
Countries
India
Contacts
Institute of Medical Sciences, Banaras Hindu University