A Clinical Trial to study the Concept of Digestive Fire and its Role in the Pathogenesis and Management of Vitiligo with Medicated Paste and Powder

To Study the Concept of Agni and its Role in the Etiopathogenesis and Principle Management (Saidhantik Chikitsa) of Shvitra Roga (Vitiligo) w.s.r. to Savarnakara Lepa and Bakuchi Churna - NIL

Status

Active, not recruiting

Phases

Phase 3Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/07/070132

Enrollment

Registered

2024-07-07

Start date

Unknown

Completion date

Unknown

Last updated

2024-07-22

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

Conditions

Health Condition 1: L00-L99- Diseases of the skin and subcutaneous tissue

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1.patients with classical sign and symptoms of the disease shvitra (vitiligo) will be selected for the study 2. patients willing and able to participate in the trial 3. patients between 15-70 years of age irrespective of gender, religion, occupation, and chronicity will be selected for the study

Exclusion criteria

Exclusion criteria: 1) Patients not willing to participate for the clinical study 2) patient below 15years and above 70 years 0f age 3) pregnant and lactating women 4 Allergy to trial drug 5) Shvitra caused due to burn were excluded

Design outcomes

Primary

Measure	Time frame
The improvement provided by the therapy will be assessed on the basis of sign and symptoms of disease 1 Twak vaivarnyam (skin changes) 2 kandu (itching) 3 Roma vivarnata (hair discolorationTimepoint: 90 days	—

Secondary

Measure	Time frame
overall improvement which will be shown by the patients in signs & symptoms of Shvitra RogaTimepoint: 110 days	—

Countries

India

Contacts

Public ContactDr Deeksha

Rajiv Gandhi government post graduate Ayurvedic college paprola Himachal Pradesh

vsonia.dogra@gmail.com7018512186

Outcome results