A study to see effect of manjisthadi lepa in treatment of hyperpigmentation.

A Single Arm Open Label Clinical Trial To Assess The Efficacy Of Manjisthadi Lepa In The Management Of Vyanga

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2020/03/023698

Enrollment

Registered

2020-03-02

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

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

Conditions

None listed

Interventions

Intervention1: Manjisthadi lepa(Manjisthadi,Vasa,Arjuntwak): To be applied daily in the morning for 30 mins with honey.Duration of the study is for 30 days(0-15th day-30th day) Control Intervention1:

Eligibility

Inclusion criteria

Inclusion criteria: Patient having signs and symptoms of vyanga

Exclusion criteria

Exclusion criteria: Hyperpigmentation caused by tumour like malingant melanoma. Patients with secondary systemic involvement. Vyanga along with kustha roga will be excluded. Pregnant and lactating women. Hyperpigmentation caused since birth is excluded because prognosis is very bad in these conditions.

Design outcomes

Primary

Measure	Time frame
To get cured of Hyperpigmentation.Timepoint: The cure shall be assessed by two follow ups in 30 days.	—

Secondary

Measure	Time frame
Getting cured of the marked symptoms on the skin adding to the cosmetic effect.Timepoint: 30 days	—

Countries

India

Contacts

Public ContactDr Jai Bhawani Babulal Barai

Dr.D.Y Patil College Of Ayurveda and Research Institute

gunvantayurved@gmail.com9028321955

Outcome results