A clinical study to see the effect of some Ayurvedic formulation in the form of nasal administration in the treatment of Vataj Shirashoola w.r.t. Headache
Phase 2
- Conditions
- Health Condition 1: R51- HeadacheHealth Condition 2: R51- Headache
- Registration Number
- CTRI/2021/02/031146
- Lead Sponsor
- Sane guruji Arogya Kendra
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1)patients suffering from symptoms of Vataj Shiashoola i.e. Shankha Ativedana, Bhru Ativedana, Lalat Ativedana
2)patients of age group 20 to 60 yrs
3)patients of eiter gender will be included in the study
4)patients yogya for Nasyakarma
Exclusion Criteria
1)patients suffering from Sinusitis,systemic disorder like Hypertension, Diabetes,
2)Secondary Headache caused by Meningitis, Tumour, Encephalitis
3)Pregnancy and Lactation
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method A clinical study to evaluate efficacy of Baladi Ghritamanda Nasya in Vataj Shirashoola w.r.t. Headache. <br/ ><br>Subjective Parameters(by using grades and Visual analogue Scale)-Shankha Ativedana,Bhru Ativedana,Lalat Ativedana <br/ ><br>Other subjective parameters-Severity of headache, Frequency of headache,Duration of headacheTimepoint: The drug will be given for 7 days.patient will be assessed before and after treatment.Total duration of study will be 18 months.
- Secondary Outcome Measures
Name Time Method Comparision between efficacy of Baladi Ghritamanda Nasya and Ksheerabala Taila Nasya in Vataj Shirashoola w.r.t. Headahe.Timepoint: Total duration of study will be 18 months