To see the effect of Kanaka tail nasya with and without local application on face in the pateints of Vyanga

An open label randomized controlled trial to evaluate the efficacy of Kanaka tail nasya with and without local application on face in the management of Vyanga - NIL

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/08/093285

Enrollment

Registered

2025-08-19

Start date

Unknown

Completion date

Unknown

Last updated

2025-09-15

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

Conditions

Health Condition 1: L811- Chloasma

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Patients having classical signs and symptoms of vyanga irrespective of gender,religion and economical status.Age group:25 years to 45 years. Patients fit for nasya karma and abhyanga.Patients willing to sign the consent form.

Exclusion criteria

Exclusion criteria: Vyanga caused due to any known systemic disease like Addison?s disease, cushing?s syndrome. Patients with known case of secondary systemic involvement like cardiac diseases etc.Vyanga along with kushta roga to be excluded.Hyper pigmentation caused by known case of tumour like malignant melanoma.Pregnant, mensurating and lactating women.Patient not fit for nasya karma and abhyanga.

Design outcomes

Primary

Measure	Time frame
Change in the grade of MASI (Melasma area severity index) score of Melasma.Timepoint: 1st - 0 Day 2nd - After completion of total 14 sittings 3rd - on follow up	—

Secondary

Measure	Time frame
Change in Colour, Size and Number of Mandalas. Change in lakshanas like Kandu, Rukshta of skin.Timepoint: 1st - 0 Day 2nd - After completion of total 14 sittings 3rd - on follow up	—

Countries

India

Contacts

Public ContactParth Kumar

Institute for Ayurved Studies and Research Shri Krishna AYUSH University

drashishhmehta@gmail.com8950375285

Outcome results