Health Condition 1: L988- Other specified disorders of the skin and subcutaneous tissue
Conditions
Interventions
Intervention1: Kanaka Tail Nasya: Group A of 34 Patients having Vyanga will be administered with Kanaka Tail Nasya 6 Drops in Each Nostril for 7 Days
Control Intervention1: Kumkumadi Tail Nasya: Group
Sponsors
PDEAs College of Ayurveda and Research Centre Akurdi
Eligibility
Inclusion criteria
Inclusion criteria: Patients having classical symptoms of vyanga like tanu niruja shyava mandal on face of patient arha for nasya
Exclusion criteria
Exclusion criteria: Known case of systemic diseases vyanga either congenital or along with kushta known case of inflammatory disease of nose
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate the efficacy of kanaka tail nasya and kumkumadi tail nasya in the management of vyanga on the basis of subjective and objective parameters within 15 daysTimepoint: Daily assessment will be done for 7 days in the duration of nasya treatment and final assessment follow up will be done on 15th day with the window period of 5 days | — |
Secondary
| Measure | Time frame |
|---|---|
| To study the adverse effects if anyTimepoint: For 7 days of nasya administration | — |
Countries
India
Contacts
Public ContactDr Sireesha Satyanarayana Popuri
PDEAs College of Ayurveda And Research Centre Akurdi
Outcome results
None listed