Single arm study to see the effect of prapunnadadi lepa in dadru kushta

Single arm clinical study to assess the efficacy of Prapunnadadi Lepa in the management of Dadru Kushta. - NIL

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/07/071233

Enrollment

Registered

2024-07-24

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: L088- Other specified local infections of the skin and subcutaneous tissue

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1)Patients diagnosed as Dadru Kushta as per sign and symptoms which are mention in Ayurvedic Samhita. 2)Gender-Irrespective of gender and socioeconomic status. 3)Age-Above 18 to 60 years.

Exclusion criteria

Exclusion criteria: 1)Pregnant women and lactating women. 2)Less than 18 years and more than 60 years. 3)Mandal with secondary infection & immuno suppressive. 4)Mandal more than 7 in number. 5)Mandal measuring above 10 cm in length and above 10 cm in breadth.

Design outcomes

Primary

Measure	Time frame
To Study the effect of Prapunnadadi Lepa in the management of Dadru Kushta.Timepoint: 10 days	—

Secondary

Measure	Time frame
1)To study Dadru Kushta in Ayurvedic perspective. 2)To study Prapunnadadi Lepa in detail in Dadru Kushta. 3)To study the efficacy of Prapunnadadi Lepa in Dadru Kushta.Timepoint: 10 days	—

Countries

India

Contacts

Public ContactDr Amruta Ramesh Rajmane

LRP Ayurvedic medical college and hospital, PG Institute and Research center, Urun Islampur Sangli

drabhinandanpatil@gmail.com9890205000

Outcome results