Clinical Study on Kajal
- Registration Number
- CTRI/2023/03/050735
- Lead Sponsor
- Sunshine Industries
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 20
1.Female subjects between the age group of 18 to 50 years.
2.Subjects who are able to give written informed consent and ready to comply with the protocol.
3.Subjects who are regular users of kajal or eye liner
1.Subjects who are visually impaired or having underlying conditions that potentially impairs their vision.
2.Subjects with known history of allergies or specific allergic reactions upon using ophthalmic cosmetic products.
3.Subjects with presenting ophthalmic conditions like dry eye, cataract, conjunctivitis etc.
4.Subjects who are regular users of prescription or cosmetic contact lens.
5.Subjects who have dark circles under their eyes.
6.Subjects who are reported pregnant/planning a pregnancy or lactating.
7.Subjects who are currently enrolled in an active investigational study or have participated in an investigational study within 30 days prior to enrolment.
8.Subjects, who in the opinion of the Investigator or the Expert Dermatologist are not eligible for enrolment in the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1.Smudge Free Hours: 16hrs <br/ ><br>2.Onset of Cooling Time: 0-5 min <br/ ><br>3.Lasting of Cooling Effect: 10-15 min <br/ ><br>4.Smearing/Fading of IP: 16-18hrs <br/ ><br>Timepoint: Day 1 to Day 2
- Secondary Outcome Measures
Name Time Method Subject IP Feedback Questionnaire: Total Score of 10Timepoint: Day 1 to Day 2