Randomised open controlled Clinical study to evaluate the efficacy of Yashtimadhu churna with Anu tail nasya in Khalitya
Trial Snapshot
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 100
- Locations
- 1
- Primary Endpoint
- To study the efficacy of Yashtimadhu churna internalywith Anu tail nasya in khalitya vyadhi
Study Overview
Brief Summary
My title is Randomised open controlled Clinical study to evaluate the efficacy of Yashtimadhu churna with Anu tail nasya in khalitya. Included the patients of classical signs and symptoms of khalitya keshapatan, keshbhumikandu,kesharukshata, visibility of scalp, hair pull test, no.of fallen hairs approximately. Treatment given Yashtimadhu churna 3gm twice a day internally for 3 months with Anu tail nasya 2 drops twice a day for 3 months to study the changes in sign and symptoms of khalitya vyadhi.
Study Design
- Study Type
- Interventional
- Allocation
- Coin toss, Lottery, toss of dice, shuffling cards etc
- Masking
- None
Eligibility Criteria
- Ages
- 18.00 Year(s) to 40.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •The patients of khalitya will be selected irrespective of occupation religion and prakriti Patient who are fit for nasya karma procedure.
Exclusion Criteria
- •Patients who are contraindicated for nasya karma procedure Patients having alopecia areata, alopecia totalis, tinea capitis, traction alopecia Patients on chemotherapy Patients of HIV and TB Serious ill patient.
Outcomes
Primary Outcomes
To study the efficacy of Yashtimadhu churna internalywith Anu tail nasya in khalitya vyadhi
Time Frame: 3 months
To decrease the keshapatan
Time Frame: 3 months
To decrease keshbhumi kandu
Time Frame: 3 months
To decrease keshrukshata
Time Frame: 3 months
Secondary Outcomes
- To study etiopathogenesis of khalitya in ayurveda & modern literature(To study the growth of hair)
Investigators
Dr Pooja Ashok Khote
Yashwant ayurvedic college post graduate training and research centre Kodoli