SUTASHEKHARA RASA FOR ORALLY AND BRIHAT JEEVAKADYA TAILA FOR NASAL DROP FOR MIGRAINE
- Conditions
- Health Condition 1: null- Patients suffering from Ardhavabhedaka
- Registration Number
- CTRI/2015/06/005940
- Lead Sponsor
- Institute for Post Graduate Teaching and Research in Ayurveda
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 30
1.Patients in the age group 20 to 60 years, presenting with signs and symptoms of Ardhavabhedaka - Migraine described as per Ayurveda and modern science will be included in the study.
2.The diagnosis of the disease shall be done on the basis of clinical manifestations like recurrent attacks of headache, mostly unilateral in site, variable in intensity, frequency and duration with or without nausea, vomiting, aura and GI tract symptoms.
1.Patients suffering from any chronic debilitating disease, with other neurological pathology, E.N.T. pathology, stress headache and cases which required surgical intervention will be excluded from study.
2.Patients suffering from Sinusitis, Hypertension, Secondary headache caused by meningitis, tumor, encephalitis, cervical spondylitis and refractive errors will be excluded from study.
3.Patients using any other systemic drugs which may alter the results of study.
4.Patients who need psychiatric treatment will be excluded.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Improvement will be assessed on the basis of <br/ ><br>relief found in cardinal symptoms of <br/ ><br>diseaseProgress in the signs and symptoms <br/ ><br>based on the standard pattern will be applied <br/ ><br>before and after treatment.Timepoint: Improvement will be assessed on the basis of <br/ ><br>relief found in cardinal symptoms of <br/ ><br>diseaseProgress in the signs and symptoms <br/ ><br>based on the standard pattern will be applied <br/ ><br>before and after treatment.
- Secondary Outcome Measures
Name Time Method Improvement will be assessed on the basis of <br/ ><br>relief found in cardinal symptoms of <br/ ><br>diseaseProgress in the signs and symptoms <br/ ><br>based on the standard pattern will be applied <br/ ><br>before and after treatment.Timepoint: 45 days