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To study the effect of Shyamadi Udvartana externally along with Varadi Churna Orally in patients suffering from fungal skin disease (Kushta -Pityriasis versicolor )

Randomised open controlled clinical trial to Evaluate the efficacy Of Shyamadi Udvartana For External application along with Varadi Churna Orally in Sidhma Kushta with special reference to Pityriasis versicolor - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/100595
Enrollment
70
Registered
2026-01-08
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Health Condition 1: B360- Pityriasis versicolor

Interventions

None listed

Sponsors

Dr Siddhi Ravindra Bhujbal
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patient having symptoms of Sidhma Kushta that is twak vaivarnya, Rajoghrushtam Vimuncchati of skin 2. Patient will be selected irrespective of gender and occupation.

Exclusion criteria

Exclusion criteria: 1.Patient with deep skin infection will excluded psoriasis, eczema, candidiasis,lichen simplex, seborrhic dermatitis 2.Patient known sensitive to sulphur preparation 3.Known history of immunocompromised patient 4.Pregnant and lactating women

Design outcomes

Primary

MeasureTime frame
To study the efficacy of Varadi churna internally along with Shyamadi Udvartana locally in Sidhma KushtaTimepoint: 30 days

Secondary

MeasureTime frame
1.To study the effect of Shyamadi Udvartana in external application and Varadi Churna internally for sign twak vaivarnya, Rajoghrushtam Vimuncchati in 30 days duration 2.To study Sidhma as per ancient ayurveda 3. To study the modern aspect of Pityriasis versicolorTimepoint: 30 days

Countries

India

Contacts

Public ContactDr Siddhi Ravindra Bhujbal

Yashwant Ayurvedic College PGT and RC kodoli

suryakiran_wagh@rediffmail.com9822846910

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026