Skip to content

Effects of a HERBAL FACE WASH in dermal safety, face dryness and fairness

Effects assessment of a HERBAL FACE WASH (a Poly Herbal Preparation) in dermal safety, dryness, and face complexions - An open level, single arm interventional study

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/10/028503
Enrollment
30
Registered
2020-10-20
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

None listed

Interventions

Intervention1: MyGlamm Wipeout HERBAL FACE WASH: The interventional product mentioned is a herbal based face wash containing the the medicinal herbs Neem, Turmeric, Tulsi, Cucumber, Sandal, Aloe Vera,

Sponsors

SANGHVI BEAUTY AND TECHNOLOGIES PRIVATE LIMITED
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Healthy male and female volunteers between 18 to 55 years of age. 2. Volunteers must be in good health. 3. Volunteers must have read and signed the Informed Consent Form. 4. Volunteers should not have any past medical history of sensitivity to the use of such products or sensitivity to the treatment constituents.

Exclusion criteria

Exclusion criteria: 1. A current skin disease of any type like eczema, psoriasis, dermatitis etc. 2. Known sensitivity to the intervention constituents. 3. Pregnant or lactating female volunteer. 4. Participation in a clinical study in the past thirty days or current participation in another similar clinical trial. 5. Unwillingness to fulfill the requirements of the study.

Design outcomes

Primary

MeasureTime frame
1. Improvement in included parameters like softness, smoothness, cleanliness, moisturizing effect on face and decrease in oiliness of the face. 2. The subject will also be evaluation in terms of lakshanas (symptoms) defined according to Ayurvedic principles like durgandhi, kandu, twaka shushkata, twakakshaya etc. These parameters were scored as poor, fair, good, very good, and excellent as per predefined visual analogue scale (VAS). Timepoint: Screening, 7th day and 14th day

Secondary

MeasureTime frame
Assessment of incidence of adverse events and patient compliance to the therapy like Irritation, Erythema, Edema, Pruritus and Urticaria and specific complications defined in Ayurveda. Timepoint: Screening, 7th day and 14th day

Countries

India

Contacts

Public ContactRuchita Tripathi Upadhyay

Department of Ayurvedic and Unani Services Uttarakhand

avnishdr@gmail.com09639017857

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026