To access the efficacy of test product for itâ??s salon fair look everyday on healthy human female subjects.

Double blinded, randomized, comparator study, to access the efficacy of test product for itâ??s salon fair look everyday on healthy human female subjects. - None

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2018/02/011784

Enrollment

Registered

2018-02-08

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: FWTS 20 and LPRC 25: Dermatologist assessment on baseline week 1 week 2 & week 4 FWTS 20 Cream 1 appox 0.5gm once in a day and LPRC 25 capsule1 entire capsule in night Control Interve

Eligibility

Inclusion criteria

Inclusion criteria: 1.Subject in generally good health. 2.Subject between the ages of 18 to 30 years. 3.Subject has done salon visits two times in the last one year for cleanup and facial. 4.Subject with Fitzpatrick III & IV skin type. 5.Subject has not participated in a similar clinical investigation in the past four weeks. 6.Subject with no known allergy/ sensitivity to cosmetic products or fragrance and without any skin allergies / infections. 7.Subject not under any dermatologic treatment / prescribed medications. 8.Subject willing to abstain from using any cosmetic product on face, besides the provided product during the entire study course. 9.Subject willing to visit the site at specified frequencies for periodic evaluations. 10.Subject willing to comply with study specific requirements. 11.Subject 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.Subject viewed by the investigator as not being able to complete the study or participating in another study.

Design outcomes

Primary

Measure	Time frame
to ascertain the salon like fairness everyday and associated skin attributes like softness, smoothness, overall appearance, glow, de-tanning, evenness etc on the healthy human female subjectsTimepoint: Baseline, week 1,week 2& week4	—

Secondary

Measure	Time frame
to ascertain the salon like fairness everyday and associated skin attributes like softness, smoothness, overall appearance, glow, de-tanning, evenness etc on the healthy human female subjectsTimepoint: Baseline, week 1,week 2& week4	—

Countries

India

Contacts

Public ContactMs Meghana Surve

The KETs Scientific research centre, Cosmetology division

meghana@kelkarcosmetology.com02225639644

Outcome results