CTRI/2025/06/088406Not yet recruitingUnknown
An In-Vivo Study to determine the Sun Protection Factor of Silphion S-1179NG
Silphion Research Private Limited1 site in 1 country10 target enrollmentStarted: June 16, 2025
Trial Snapshot
- Phase
- Unknown
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 10
- Locations
- 1
- Primary Endpoint
- Change in Individual MED (iMED) score
Study Overview
Brief Summary
This is the Invivo SPF test done as per UV-B protection ISO 24444 to determine the Sun Protection Factor
Test Product:
1. S-1179NG
Done on 10 human volunteers. Duration: 3 Days
Study Design
- Study Type
- Observational
Eligibility Criteria
- Ages
- 18.00 Year(s) to 65.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •Individual should have ITA angle in the range of 18 t0 40, 41 to 55, and greater than 56
- •Individuals free of any dermatological or systemic disorder which would interfere with the results, at the discretion of the investigator.
- •Individuals who have completed a preliminary medical history evaluation.
- •Individuals who have read, understood and signed an informed consent document relating to the specific study to which they are subscribing.
- •Individuals with no known abnormal response to sunlight.
Exclusion Criteria
- •1.Individuals taking medication which in the opinion of the investigator would mask or interfere with the results.
- •2.Individuals with chronic skin allergies.
- •3.Individuals with suntan or sunburn.
- •4.Individuals with abnormal reaction to the sun.
- •5.Pregnant or lactating females.
- •6.Subjects accustomed to using sun beds.
- •7.Subjects who have participated in an SPF study within the last two months.
Outcomes
Primary Outcomes
Change in Individual MED (iMED) score
Time Frame: Day1, Day2
Secondary Outcomes
- Not Applicable(Not Applicable)
Investigators
Study Sites (1)
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