Effect of Munditika Yog and Apamarga Taila Nasya in the Management of Ardhavbhedak w.s.r. to Migraine
- Conditions
- Health Condition 1: R908- Other abnormal findings on diagnostic imaging of central nervous system
- Registration Number
- CTRI/2024/07/069737
- Lead Sponsor
- Madan Mohan Malviya Govt Ayurved College
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
i)Patients having a history of migraine as defined by Ayurveda classics and International Headache Society, at least one year prior to enrollment and chronicity not exceeding more than five years.
ii)Patients willing for trial with consent.
iii)Age between 18 to 60 years.
iv)Either sex of different socio-economic groups.
i)Age below 18 or more than 60 years.
ii)Patients of Ardhavbhedak who are taking other preventive treatment.
iii)Patients who are suffering from other chronic diseases.
iv)Patients who are suffering from secondary headache of meningitis, brain tumor, encephalitis or having referred pain on one half of the head due to disorders of eye, ear, nose, throat, etc.
v)Patients with previous completion or withdrawn from the study.
vi)Evidence of significantly active psychiatric disease including manic depressive illness, schizophrenia, generalized anxiety disorder, OCD, and personality disorder.
vii)Women who are pregnant or nursing.
viii)Excessive alcoholic and with history of drug dependence or drug abuse.
ix)Hypersensitive to any of the trial drugs or their ingredients.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Aradhashirovedna (unilateral headache), Prakash asahishnuta (Photophobia), Dhwani asahishnuta (Phonophobia), Bhram (Vertigo), Nausea, Vomiting, Severity, freuency and duration of headache wil be analysed <br/ ><br>g)Tinnitus <br/ ><br>Timepoint: On 45 day after registration of patients
- Secondary Outcome Measures
Name Time Method Reduction in signs & symptoms with improved quality & vitality of life.Timepoint: At 15, 30 & 45 day after registration of patient.