A clinical trial to compare the efficacy of pracchana & pracchana followed by durvadya taila application in vicharchika w.s.r. dry eczema

A comparative clinical study to evaluate the efficacy of pracchana & pracchana followed by durvadya taila application in vicharchika w.s.r. to dry eczema

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2023/06/054484

Enrollment

Registered

2023-06-27

Start date

Unknown

Completion date

Unknown

Last updated

2023-07-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: L309- Dermatitis, unspecified

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1)Patients presenting with classical signs & symptoms of Vicharchika w.s.r. dry eczema of either sex will be selected irrespective of their occupation 2)Patients between the age group 18-70 years. 3)Lesions over hands, legs, feet, cubital and popliteal regions.

Exclusion criteria

Exclusion criteria: 1)Patients suffering from Systemic diseases like uncontrolled DM, HTN, Cardiac illness, Anemia. 2)Patients with bleeding disorders. 3)Patients on anti-coagulant and anti-platelet drugs 4)Pregnant women & Lactating women. 5)Patients suffering from Immunocompromised diseases. 6)Vicharchika associated with other skin disorders.

Design outcomes

Primary

Measure	Time frame
Reduction in the dryness & area of eczemaTimepoint: 21 days	—

Secondary

Measure	Time frame
To assess parameters like reduction in the dryness, area, itching, discoloration, excoriation, lichenification of eczemaTimepoint: 21 days	—

Countries

India

Contacts

Public ContactDr Srinivas Masalekar

Government Ayurvedic Medical College and Hospital Bengaluru

drvasudha.a@gmail.com9480365291

Outcome results