Health Condition 1: G439- Migraine, unspecified
Conditions
Interventions
Intervention1: A comparative experimental study to assess the efficacy of
administration of individualised homoeopathic medicine in solid
globule form and liquid dilution form in treatment
of migrai
Sponsors
Sainath Hospital
Eligibility
Inclusion criteria
Inclusion criteria: Diagnosed cases of migraine based on International Classification of Headache Disorders (ICHD-3). Willing to give written informed consent. Able to comply with research and follow ups.
Exclusion criteria
Exclusion criteria: Patients with other types of headache (tension-type, cluster, etc.). Any Known psychiatric disorders Pregnant or lactating women. Participation in other study within the last 3 months
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Reduction in migraine-related disability or pain measured by MIDAS score.Timepoint: Baseline(Day 0) Follow up every 15 days up to 12 months | — |
Secondary
| Measure | Time frame |
|---|---|
| Change in frequency and intensity of migraine attacks during the study period. Patient compliance with prescribed mode of medicine administration (globule vs. liquid). Patient satisfaction with treatment form assessed through feedback. Recurrence rate of migraine episodes during the 12-month follow-up.Timepoint: Baseline (Day 0) Follow-up every 15 days up to 12 months | — |
Countries
India
Contacts
Public ContactSantoki Bhavik Lavjibhai
Rajkot Homoeopathic Medical College
Outcome results
None listed