A comparative clinical trial of efficacy of Agnikarma with and without Laghusutashekhra rasa in the management of Ardhavabhedaka w.s.r. to Migraine without aura
- Conditions
- Health Condition 1: G09- Sequelae of inflammatory diseasesof central nervous system
- Registration Number
- CTRI/2024/05/067272
- Lead Sponsor
- Shekh Afreen Naaz
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1. Patients between age group 18 to 60 years.
2. Patient’s fulfilling the diagnostic symptoms of Ardhavbhedaka like - recurrent attacks of headache(shirovedana), mostlyunilateral in site, variable in intensity, frequency and duration with or without nausea (hrullasa), vomiting (chardi), vertigo (bhrama) will be selected
randomly irrespective of age, sex, religion and occupation.
3. Patients fit for Agnikarma.
1. Any other known systemic disorders which will affect or
interfere course of treatment e.g., Hypertension, DM
2. Patient’s not fit for Agnikarma19
.
3. Secondary headache caused due to meningitis, encephalitis,
cervical spondylosis.
4. Referred pain due to diseases of eye, ear, nose, teeth etc.
5. Patients with complicated migraine that is complications
like loss of hearing, loss of vision.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Reduction in classical sign & symptoms of ArdhavbhedakaTimepoint: 7th, 14th, 21st and 28 th day and post treatment 15th day
- Secondary Outcome Measures
Name Time Method 1. To compare the efficacy of Agnikarma and Laghusutashekhara <br/ ><br>rasa along with agnikarma in the management of Ardhavabhedaka <br/ ><br>w.s.r. to Migraine without aura. <br/ ><br>2. To evaluate combined efficacy of Laghusutashekhara rasa along <br/ ><br>with agnikarma in the management of Ardhavabhedaka w.s.r. to <br/ ><br>Migraine without aura.Timepoint: 7th, 14th, 21st and 28 th day and post treatment 15th day