MedPath

A study to evaluate efficacy and safety of the test product on the tanned skin.

Not Applicable
Registration Number
CTRI/2024/07/071206
Lead Sponsor
Zydus Wellness Products Limited
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1)Subjects with fitzpatrick skin type IV and V.

2)Subjects with visible skin tan on face, at least 2 shade darker than a Sun protected upper volar arm.

3)Subjects with visible blackheads on the face.

4)Subjects with at least 2 dark spots / blemishes.

5)Subjects willing to provide written informed consent to participate in the study.

Exclusion Criteria

1)Subjects with dark facial skin as determined by dermatologist.

2)Subjects who are receiving topical or systemic treatments for pigmentation within the last 30 days.

3)Subjects using other marketed skin lightening products during the study period or in the past 6 weeks.

4)Subjects using any other facial scrub during the study period.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To assess the efficacy of test product on tanned skin, based on clinical, instrumental and subjective evaluationsTimepoint: Day 01, Day 03, Day 07, Day 14 and Day 28.
Secondary Outcome Measures
NameTimeMethod
ILTimepoint: NI
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