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To see the effect of applying adaki and masoor dal in improving the overall skin quality of the face.

A Randomised Comparative Clinical Trial To Assess The Efficacy And Tolerability Of Local Application Of Adhaki Dal Cajanus cajan L Millsp And Masoor Dal Lens Culinaris Medik For Varnya Effect With Special Reference To Overall Skin Quality In Apparently Healthy Volunteers - nil

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/04/108497
Enrollment
70
Registered
2026-04-16
Start date
Unknown
Completion date
Unknown
Last updated
2026-04-27

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

National Institute of Ayurveda, Deemed to be University
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Volunteers meeting the following criteria will be enrolled: Between the age of 18-35 years (male and female) Individuals who are willing to provide written informed consent Individuals who agree not to wear makeup or use skin care products other than the study products the day of the study visits Individuals willing to discontinue using current skin care products and only use study products for the study duration Individuals willing to refrain from sun tanning / sun bathing for the study duration

Exclusion criteria

Exclusion criteria: Volunteers will be excluded from the study if they meet any of the criteria listed below: Any medically diagnosed chronic skin problems on their face (e.g., psoriasis, eczema, dermatitis, or chronic cystic acne, etc.) Diagnosed with known allergies to facial skin care products Have undergone dermatological skin rejuvenation procedures such as light-therapies (lasers, radio frequency and other lights treatments ) or such as collagen or other facial tissue augmentation, fillers, or retail micro abrasion on the face within the last 1 year preceding the baseline visit and intended to receive them during the study period Have planned surgeries or invasive procedures during the course of the study.

Design outcomes

Primary

MeasureTime frame
Improved radiance and luminosity Reduced dullness Improved skin texture Even skin tone Fading dark spot Timepoint: at baseline, 4 weeks

Secondary

MeasureTime frame
nillTimepoint: nill

Countries

India

Contacts

Public ContactDr Sumit Nathani

National Institute of Ayurveda, Deemed to be University

sumitnathani2@rediff.com8005789294

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: May 1, 2026