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standardization and quality evaluation of ayurvedic kumkumadi taila,and its lotion,comparative clinical evaluation in the management of vyanga(melasma)

Pharmaceutico--analytical standardization of Kumkumadi Taila and its modification into lotion form with comparative clinical evaluation in Vyanga(Melasma) - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/06/112737
Enrollment
60
Registered
2026-06-15
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

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

Sponsors

Institute of teaching and research in Ayurveda ,jamnagar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Having classical signs symptoms of Vyanga like Tanuka, Shyava and Mandala. Uncomplicated Participants cases with classical signs and symptoms of Vyanga will be selected irrespective of gender, religion, profession.

Exclusion criteria

Exclusion criteria: Participants receiving hormonal or corticosteroid therapy. Participants with history of endocrine disorders or allergies. Participants taking depigmenting or whitening products (oral or topical) within the previous 2 weeks will also be excluded. Participants with known allergy to any component of Kumkumadi Taila and Lotion. Pregnant women will be excluded.

Design outcomes

Primary

MeasureTime frame
Comparative evaluation of clinical efficacy of Kumkumadi Taila and its lotion.Timepoint: 1.5 years—

Secondary

MeasureTime frame
Pharmaceutical standardization & analytical profile development of Kumkumadi Taila and its lotion. Timepoint: 1 years—

Countries

India

Contacts

Public ContactDrJoban Modha

Institute of teaching and research in Ayurveda,jamnagar

jobanm@itra.edu.in9825273008

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 29, 2026