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Evaluation of the safety and efficacy of the Toomar herbal facial mask

Evaluation of the safety and efficacy of the Toomar herbal facial mask for skin rejuvenation and depigmentation

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190210042676N48
Enrollment
20
Registered
2025-12-19
Start date
2025-12-21
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

Skin aging. Changes in skin texture

Interventions

Intervention group: Use of the Toumaar herbal powder facial mask as follows: half a teaspoon of the powder is mixed with half a small glass of boiling water to form a soft paste. The resulting paste i

Sponsors

Asna Teb Ariyai Company
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 60 Years

Inclusion criteria

Inclusion criteria: Women or men aged 30 to 60 seeking facial skin rejuvenation and brightening. Provision of written informed consent by the volunteer to participate in the study, compliance with the applicable requirements, and willingness to attend regular follow-up visits.

Exclusion criteria

Exclusion criteria: Use of any photosensitizing medication within 3 months prior to the start of treatment. Active skin conditions in the test area: acne, eczema, atrophy, and rosacea Use of topical brightening products such as AHA (alpha hydroxy acid) and BHA (beta hydroxy acid) compounds and those containing retinoids 21 days before the study Having another skin condition with hyperpigmentation symptoms such as melasma or freckles Sensitivity to any of the ingredients in the product

Design outcomes

Primary

MeasureTime frame
Overall facial condition in terms of brightening, reduction of pore size, and improvement of fine skin wrinkles. Timepoint: Before the intervention and 28 days after the intervention. Method of measurement: Assessment of before-and-after photographs by an independent physician using the GAIS(Global AestheticImprovement Scale).

Secondary

MeasureTime frame
Stratum corneum hydration. Timepoint: Before the intervention, and at 14 and 28 days after the intervention. Method of measurement: Corneometery.;Number, extent, and percentage of skin spots. Timepoint: Before the intervention, and at 14 and 28 days after the intervention. Method of measurement: Visioface.;Skin elasticity. Timepoint: Before the intervention, and at 14 and 28 days after the intervention. Method of measurement: Catometery.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAniseh Samadi

Tehran University of Medical Sciences

aniseh_samadi@yahoo.com+98 21 8896 0880

Outcome results

None listed

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