A Clinical Study to Evaluate the moisturization potential of Deep Revitalise Hydration creme- Normal combination skin
Overview
- Phase
- Post Marketing Surveillance
- Status
- Not yet recruiting
- Sponsor
- Honasa Consumer Limited
- Enrollment
- 32
- Locations
- 1
- Primary Endpoint
- 1. Change in Skin Hydration
Overview
Brief Summary
A single blind one arm study.
Each participant entering the trial will be assigned to a regimen of investigational product at marked Test product box and no product at the other box.
Assessment Time: Day 0 (T0min, T+30 mins), 4 hour, 8 hour, Day1 and Day 14
Assessments:
-
Skin Hydration with Corneometer [Day 0 (baseline and 30min), Day 1 and Day 14]
-
TEWL with Tewameter. [Day 0 (baseline and 30min) and Day 14]
-
Dermascopy with 9 point dermat evaluation for skin texture smoothness Score. [Day 0 (baseline and 30min) and Day 14] (with images)
-
How many hours of Balanced & Weightless Hydration for Smooth Skin was observed?- Day 14
-
T-zone comfort test- consumer questionnaire- yes/No?- Day 14
Study Design
- Study Type
- Pms
- Allocation
- Na
- Masking
- None
Eligibility Criteria
- Ages
- 20.00 Year(s) to 35.00 Year(s) (—)
Inclusion Criteria
- •Gender: Male or Female with age 20-
- •Subjects having Normal to Combination skin only.
- •Subjects willing to give written informed consent 4) Women of child bearing potential must have a negative urine pregnancy test prior to study entry.
- •Are free of any systemic or dermatologic disorder, which, in the opinion of the investigator, will interfere with the study results or increase the risk of adverse events.
- •Are willing to avoid prolonged exposure of the treatment area to ultraviolet radiation (natural or artificial) for the duration of the study.
Exclusion Criteria
- •Subjects who are pregnant, breast-feeding, or planning to become pregnant during the study.
- •Have any evidence of systemic cancer, squamous cell carcinoma, basal cell carcinoma, in the last 5 years, or any other confounding skin condition.
- •Have open sores or open lesions in the treatment area(s).
- •Have any condition that, in the opinion of the investigator, would confound the safety and efficacy assessments of the product.
- •Have participated in any interventional clinical trial in the previous 90 days.
- •Have a known sensitivity to any of the constituents of the test product.
- •Have used, are using, or are planning to use immunosuppressive or immunomodulatory medication (i.e.,biologics), including corticosteroids.
- •Have not skin related issues.
Outcomes
Primary Outcomes
1. Change in Skin Hydration
Time Frame: Time Points: Day 0 (T0min, T+30 mins), 4 hour, 8 hour, Day1 and Day 14
2. Change in TEWL with Tewameter
Time Frame: Time Points: Day 0 (T0min, T+30 mins), 4 hour, 8 hour, Day1 and Day 14
3. Change in smoothness Score
Time Frame: Time Points: Day 0 (T0min, T+30 mins), 4 hour, 8 hour, Day1 and Day 14
Secondary Outcomes
- Not Applicable(Not Applicable)
Investigators
Dr Robin Chugh
CCFT Laboratories