None listed
Conditions
Interventions
Intervention1: NIL: NIL
Control Intervention1: NIL: NIL
Sponsors
ITC R D Centre
Eligibility
Inclusion criteria
Inclusion criteria: •Subjects willing to give written informed consent and abide by the study protocol. •10 healthy female subjects in the age group of 20 to 50 yrs. •At least 5 subjects with cellulite on at least one of the arms/ thighs and the remaining 5 with normal skin. •Subjects with no medical history of disease / medical condition/ concurrent illness/ pre-existing or dormant dermatologic condition that could interfere with the study results. •Subjects who are not pregnant or nursing. •Subjects who are willing to abstain from using any cosmetic product on the identified sites on the day of study.
Exclusion criteria
Exclusion criteria: • Subjects who are pregnant or lactating. • Subjects having skin disease (e.g. psoriasis, atopic dermatitis or other cutaneous manifestations), which would interfere with the test readings. • Subjects on medications (e.g. steroids or antihistamines), which could compromise the study results. • Subjects with scars, cuts/ wounds/ scratches on the potential test sites (Brachium region, Femoral regions and Volar forearm), which could interfere with the test readings.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To study for difference in skin thickness, moisture, elasticity, viscoelasticity, smoothness, firmness and color recovery in cellulite accumulated skin vs. non cellulite accumulated skin through non-invasive instrumental measurements and visual evaluation.Timepoint: single visit evaluation | — |
Secondary
| Measure | Time frame |
|---|---|
| To study the correlation between the varied evaluation tools available to measure skin cellulite.Timepoint: Single visit evaluation | — |
Countries
India
Contacts
Public ContactDr SapnaR
MS Clinical Research Pvt.Ltd.
Outcome results
None listed