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To the effect of IDC products on dark spots on face and neck.

Phase 4
Completed
Conditions
Health Condition 1: null- hyper pigmentation/dark spots of the face and neck.
Registration Number
CTRI/2012/02/002434
Lead Sponsor
Glenmark Pharmaceuticals Ltd
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
20
Inclusion Criteria

Subjects with hyper pigmentation/dark spots of the face and neck.

Age group: 30 years and above

Willing to restrain from prolonged exposure to the sun for the length of the study

Available for the entire duration of the study

Exclusion Criteria

Hypersensitivity to any ingredients

Pregnant and lactating women.

Subjects who are already applying anti-aging, skin lightening or AHA (Alpha hydroxy acids) based or retinol based cosmetics or have applied any of these in the last 3 months.

Subjects with dermatological disorder of face that may interfere with study evaluation.

Subjects who have undergone any surgical treatment of the face.

Study & Design

Study Type
PMS
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
improvement in spots darkenss MASI scoring <br/ ><br>Physicians Global Assessment Grade for improvement in complexion / dark spots on the face and neck <br/ ><br>Patients Global Assessment Grade for improvement in complexion / dark spots on the face and neck <br/ ><br>Quality of life Questionnaire <br/ ><br>Patient Satisfaction Questionnaire <br/ ><br>Timepoint: 12 weeks
Secondary Outcome Measures
NameTimeMethod
ILTimepoint: NI
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