SPF of Esthetic Sunscreen-Sample 1

An In-Vivo study to Determine the Sun Protection Factor of Esthetic Sunscreen-Sample 1 - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Observational

Source

CTRI

Registry ID

CTRI/2026/02/102941

Enrollment

Registered

2026-02-04

Start date

Unknown

Completion date

Unknown

Last updated

2026-03-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Intervention1: Test Product: Sunscreen-Sample 1: Quantity 2 mg/sq.cm Route of administration: Topical Frequency: Once Duration: 24 hour Control Intervention1: Not Applicable: Not Applicable

Eligibility

Inclusion criteria

Inclusion criteria: 1. Individual should have ITA angle in the range of 28 t0 40, 41 to 55, and greater than 56 2. Individuals free of any dermatological or systemic disorder which would interfere with the results, at the discretion of the investigator. 3. Individuals who have completed a preliminary medical history evaluation. 4. Individuals who have read, understood and signed an informed consent document relating to the specific study to which they are subscribing. 5. Individuals with no known abnormal response to sunlight.

Exclusion criteria

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.

Design outcomes

Primary

Measure	Time frame
Change in Individual MED (iMED) scoreTimepoint: Day1, Day2, Day3	—

Secondary

Measure	Time frame
Not ApplicableTimepoint: Not Applicable	—

Countries

India

Contacts

Public ContactPuneet Mittal

CCFT Laboratories

puneetmittal@mgcts.org08937015757

Outcome results