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To evaluate the efficacy of face wash, face scrub and face mask when used in combination, to give Clear pores effect on healthy female subjects.

A double blinded, single centered study to evaluate the efficacy of face wash, face scrub and face mask when used in combination, to give Clear pores effect on healthy female subjects.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2013/02/003419
Enrollment
40
Registered
2013-02-21
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: CPF â?? 01: (Face Wash- twice a day)Assessment of dermatologist and subject self assessment on Baseline (week 0), week 1, week 2 and week 4 Assessment of dermatologist and subject self

Sponsors

Hindustan Unilever Limited
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Volunteer in generally good health. 2.Volunteer between the ages of 18 to 30 years. 3.Volunteer with mild to moderate acne condition with a few Blemishes. 4.Volunteer has not participated in a similar clinical investigation in the past four weeks. 5.Volunteer with no known allergy/ sensitivity to cosmetic products or fragrance and without any skin allergies / infections. 6.Volunteer not under any dermatologic treatment / prescribed medications. 7.Volunteer willing to abstain from using any cosmetic product on face, besides the provided products during the entire study course. 8.Volunteer willing to visit the site at specified frequencies for periodic evaluations. 9.Volunteer willing to comply with study specific requirements. 10.Volunteer willing to give a written informed consent and come for regular observation.

Exclusion criteria

Exclusion criteria: 1.A known history or present condition of allergic response to any cosmetic products. 2.Skin disease (e.g. psoriasis, atopic dermatitis or other cutaneous manifestations on the scalp), which would interfere with the test readings. 3.Medications (e.g. steroids or antihistamines), which would compromise the study. 4.Currently or has been undergoing dermatologist facial treatments or procedures within the last 1 month. 5.Volunteer viewed by the investigator as not being able to complete the study or participating in another study. 6.Pregnant or lactating.

Design outcomes

Primary

MeasureTime frame
The objective of this study is to ascertain the clear pores and associated skins attributes like Prevention from breakouts, fights blemishes, reduces irritation, removes excess oil, gives clear and mattified skin, tighten pores, gives soft and smooth skin, improves overall appearance, glow, evenness etc on the healthy human female subjects.Timepoint: Baseline (week 0), week 1, week 2 and week 4

Secondary

MeasureTime frame
The objective of this study is to ascertain the clear pores and associated skins attributes like Prevention from breakouts, fights blemishes, reduces irritation, removes excess oil, gives clear and mattified skin, tighten pores, gives soft and smooth skin, improves overall appearance, glow, evenness etc on the healthy human female subjects.Timepoint: Baseline (week 0), week 1, week 2 and week 4

Countries

India

Contacts

Public ContactMs Meghana Surve
meghana@kelkarcosmetology.com9102225639644

Outcome results

None listed

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