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Clinical Study on DESA AYURVEDA PRODUCTS in Healthy participants.

Evaluation of safety and overall sensory attributes of DESA AYURVEDA PRODUCTS in Healthy Subjects. - NIL

Status
Recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/05/110300
Enrollment
30
Registered
2026-05-10
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

None listed

Interventions

None listed

Sponsors

HOUSE OF ADITI PRIVATE LIMITED
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Healthy males and females (Healthy individuals will be defined as those who are not taking any medications and do not require continuous medical care and monitoring) 2. Willing to comply with all requirements of the study

Exclusion criteria

Exclusion criteria: 1. Healthy males and females (Healthy individuals will be defined as those who are not taking any medications and do not require continuous medical care and monitoring) 2. Willing to comply with all requirements of the study Exclusion criteria 1. Subjects with a known current history of chronic skin diseases or autoimmune diseases, such as atopic dermatitis, psoriasis, chronic urticaria, vitiligo and rosacea 2. Subjects with a tattoo, a scar, moles, too many hairs or evaluation area which might interfere with the evaluation. 3. Subjects with intensive exposure to sunlight or UV rays within the previous month and foreseen during the study. 4. Subjects who have used facial blemish-lightening products (such as products claiming to have whitening or blemish-lightening effects), topical or oral whitening drugs. Moisturizing cream, lotion or oil within 21 days before entering the trial 5. Subjects on any other investigational products within 1 month prior to randomization 6. Subjects with known current tuberculosis, HIV, ischemic heart disease, cancer, kidney failure, liver failure 7. Pregnant and lactating women 8. Known hypersensitivity to any of the ingredients of study products 9. Other conditions, which in the opinion of the investigators, make patient unsuitable for enrolment or could interfere with his or her participation in, and completion of the study

Design outcomes

Primary

MeasureTime frame
Assessment of skin patch test using Dermal Response ScoreTimepoint: 15-30 minutes, 24 hours post application, 48 hours post application

Secondary

MeasureTime frame
1 Assessment of appearance, fragrance intensity, spreadability, absorption, skin finish, Hair finish, Greasy feel, Comfort level, overall sensory satisfaction after one time application of Desa Face Wash, Desa Face pack, Desa Vetiver Spray, Desa Hair Cleanser, Desa Hair Oil, Desa Parijat Body Oil, Desa Vanilla Mandarin Body Oil and Desa Hair Conditioner. 2 Assessment of adverse events/adverse drug reactions including vitals Timepoint: Post application assessment

Countries

India

Contacts

Public ContactDr Sanjay Tamoli

Target Institute of Medical Education and Research Pvt Ltd

targetinstitute@yahoo.com9322522252

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 11, 2026