To test the safety and benefits of the hydration mist on all type skin.
Not Applicable
Completed
- Registration Number
- CTRI/2023/05/052949
- Lead Sponsor
- DPKA Universal Consumer Ventures Private Limited
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 50
Inclusion Criteria
• Healthy female subjects of 18 to 50 years age. Include subjects with all skin types
• Non-pregnant/non-lactating females.
• Subject who had normal Fitzpatrick skin type III to V.
Exclusion Criteria
• Subjects who are pregnant, breast feeding or planning a pregnancy
• Subjects who have demonstrated a previous hypersensitivity reaction to any of the ingredients of the
study products.
• Medication which may affect skin response and/or past medical history as determined by the
investigator
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. Hydration of bare face by Derma Lab Combo before treatment of hydrating mist (0 min), 30 mins and 4hrs after treatment will be evaluated. <br/ ><br>2. 30 mins post application of make up or when considered set by the make-up artist spray the hydrating mist as directed & fill the response form the subjects <br/ ><br>3. Digital images of the bare face and make up are taken before the treatment with hydrating mist (0 min) and 30 mins after treatment with hydrating mist. <br/ ><br>4. Clinical efficacy graded by Griffiths scale is scored before the application of hydrating mist (0 min), 30 min and 4 hr. after application of the hydrating mist on bare face.Timepoint: Day 1 <br/ ><br>Bare Face: 0 min, 30 min, 04 Hours <br/ ><br>Make up Face: 0 min, 30 min <br/ ><br>
- Secondary Outcome Measures
Name Time Method ot ApplicableTimepoint: Not Applicable