Vicharchikari Taila in treatment of Vicharchika

Pharmaceutical Standardization And clinical Evaluation On Vicharchikari Taila In The Management Of Vicharchika. - NIL

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/07/071580

Enrollment

Registered

2024-07-30

Start date

Unknown

Completion date

Unknown

Last updated

2024-08-19

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

Conditions

Health Condition 1: L089- Local infection of the skin and subcutaneous tissue, unspecified

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients 14-70 years of both sexes will be selected 2. Patients fulfilling the criteria of classical symptoms of Vicharchika like Kandu (Itching), Pidika (Papillae), Shyavavarna (Discoloration), Daha (Burning sensation), Rukshta (Dryness) and Ruja (Pain) will be selected for assessment. 3.Patients having complaints for less than 5 years.

Exclusion criteria

Exclusion criteria: 1.Patients below 14 and above 70 years. 2.Patients having complaints for more than 5 year. 3.Patients having pregnancy 4.Patient having any allergic history or sensitivity will be excluded from study 5.Patient having diabetes, will be excluded from present study.

Design outcomes

Primary

Measure	Time frame
Relive in classical symptoms of Vicharchika.Timepoint: 60 days	—

Secondary

Measure	Time frame
Repigmentation and decrease in relapsing lesion of atopic dermatitis.Timepoint: 60 days	—

Countries

India

Contacts

Public ContactDr Palak Sharma

Postgraduate Institute Of Ayurveda

dr.govindshukla@yahoo.com08769058254

Outcome results