Health Condition 1: L088- Other specified local infections of the skin and subcutaneous tissue
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Patients between 10 to 16 years of age irrespective of gender. 2.Patients with clinical signs of the disease Sidhma Kushtha (Pityriasis Versicolor)- Rajoghrishtma vimunchyati (Furferaceous scales) Tamra Varna (Reddish black,brown coloured macules) AlabupushpaVarna(Hypopigmentedmacules/hyperpigmented macules) Kandu (Itching) Urdhav kaye especially Uras (chest, trunk or neck) Tanu (thin plaques) 3. Patients found positive for KOH test 4. Willing to give assent/consent for the trial
Exclusion criteria
Exclusion criteria: 1.Children with congenital anomalies, chronic ailments such as tuberculosis, malignancy, cardiac, and renal disorders, autoimmune disorder or any other systemic illness 2.Patient have received systemic antifungal therapy within 1 month or topical antifungal therapy within 1 week of the commensal of study. 3.Patients with vitiligo, leprosy, pityriasis rosea, psoriasis, pityriasis alba, tinea capitis, tinea cruris any other skin disease 4.Parents of the patient not willing to participate in the trial
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1 Antifungal effect of Tuvarak taila cream by performing KOH test. 2 Efficacy of Tuvarak taila cream in management of clinical features of Sidhma kushtha (pityriasis versicolor). Timeframe On 14th day/21st day (AT)and 42nd /49th day (FU). (Expected 90% improvement) and improvement in clinical features of Sidhma kushtha as per classical texts of Ayurveda Timepoint: 1 Antifungal effect of Tuvarak taila cream by performing KOH test. 2 Efficacy of Tuvarak taila cream in management of clinical features of Sidhma kushtha (pityriasis versicolor). i.e. Timeframe On 14th day/21st day (AT)and 42nd /49th day (FU). (Expected 90% improvement) and improvement in clinical features of Sidhma kushtha as per classical texts of Ayurveda | — |
Secondary
| Measure | Time frame |
|---|---|
| 1.Improvement in quality of life of the child as per Children’s Dermatological Life Quality Index (CDLQI) (Expected 90% improvement)Timepoint: AT (3weeks for group 1) & (2weeks for group 2) Follow Up After 4 weeks for both groups i.e.(7weeks for group 1) & (6weeks for group 2) | — |
Countries
India
Contacts
ALL INDIA INSTITUTE OF AYURVEDA