Skip to content

Markavyuktakshir Nasya for vyanga(melasma) patients for 15 days

An exploratory clinical study to evaluate the efficacy of Markavyukta ksheer Nasya in the management of vyanga - Nil

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/11/060205
Enrollment
45
Registered
2023-11-23
Start date
Unknown
Completion date
Unknown
Last updated
2023-12-19

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

Conditions

Health Condition 1: L578- Other skin changes due to chronicexposure to nonionizing radiation Health Condition 2: L55-L59- Radiation-related disorders of the skin and subcutaneous tissue

Interventions

None listed

Sponsors

PDEAS college of ayurved and research centre Nigadi pune
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients showing classical signs and symptoms of vyanga like tanu, niruja, shyava mandal on face. 2. Patients of age between 25 to 55 years irrespective of gender, religion and economic status

Exclusion criteria

Exclusion criteria: 1. Vyanga caused due to any known systemic disease like Addison’s disease, Cushing’s syndrome. 2. Vyanga caused since birth like Nevus of Ota 3. Vyanga along with kushta roga 4. Hyper pigmentation caused by known case of tumour like malignant melanoma 5. Pregnant and lactating women 6. Patient’s anarha for nasya karma

Design outcomes

Primary

MeasureTime frame
To Evaluate efficacy of markavyuktakshir nasya in management of vyanga for 15 daysTimepoint: 3 follow ups will be taken on 7th,15th and 21th day and the treatment will be given for 15 days

Secondary

MeasureTime frame
To observe the adverse effect if any for 15 daysTimepoint: 15 days study with 3 folow ups 7th, 15th and 21th day

Countries

India

Contacts

Public ContactShubhangi maske

Pdeas College of ayurved and research centre nigadi pradhikaran pune

Rikibepournima@gmail.com9762561699

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026