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Sunscreen Agents clinical trials

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NCT ID: NCT05004168 Completed - Sunscreen Agents Clinical Trials

Sun Protection Factor (SPF) / UVA Protection Factor Study

Start date: September 2, 2020
Phase: N/A
Study type: Interventional

Evaluation of the effectiveness of sunscreen products by determining its Sun Protection Factor (SPF) against UV-B and UV-A

NCT ID: NCT02885805 Completed - Sunscreen Agents Clinical Trials

Sun Protection Factor (SPF) Efficacy Assay

Start date: June 26, 2015
Phase: N/A
Study type: Interventional

Evaluation of the effectiveness of a sunscreen product by determining its Sun Protection Factor (SPF) on the skin of human subjects.

NCT ID: NCT02872246 Completed - Sunscreen Agents Clinical Trials

Sun Protection Factor (SPF) / UVA Protection Factor (UVAPF) - Assay

Start date: May 26, 2015
Phase: N/A
Study type: Interventional

Evaluation of the effectiveness of a sunscreen product by determining its Sun Protection Factor (SPF) on the skin of human subjects.

NCT ID: NCT02872233 Completed - Sunscreen Agents Clinical Trials

Sun Protection Factor (SPF) / UVA Protection Factor (UVAPF) Assay

Start date: May 26, 2015
Phase: N/A
Study type: Interventional

Evaluation of the effectiveness of a sunscreen product by determining its Sun Protection Factor (SPF) on the skin of human subjects.

NCT ID: NCT02872207 Completed - Sunscreen Agents Clinical Trials

Evaluation of the Stinging Potential in Human Eyes

Start date: February 21, 2015
Phase: N/A
Study type: Interventional

The objective of this study was to compare the human eye stinging potential of experimental formulas and an industry standard shampoo mixture. The study was conducted under the supervision of a Board Certified Ophthalmologist.

NCT ID: NCT02872194 Completed - Sunscreen Agents Clinical Trials

Evaluation of the Stinging Potential of Products in Human Eyes

Start date: September 5, 2014
Phase: N/A
Study type: Interventional

The objective of this study was to compare the human eye stinging potential of experimental formulas and an industry standard shampoo mixture. The study was conducted under the supervision of a Board Certified Ophthalmologist. The study design was a three cell, single blind study. Subjects were given the industry standard shampoo mixture in one eye and an exploratory sunscreen in the other as according to the randomization schedule.

NCT ID: NCT02869113 Completed - Sunscreen Agents Clinical Trials

Evaluation of the Stinging Potential of Sunscreen Products in Human Eyes

Start date: January 23, 2015
Phase: N/A
Study type: Interventional

The objective of this study was to compare the human eye stinging potential of experimental formulas and an industry standard shampoo mixture. The study was conducted under the supervision of a Board Certified Ophthalmologist.

NCT ID: NCT02857738 Completed - Sunscreen Agents Clinical Trials

Sun Protection Factor (SPF) - Static and Water Resistant Assay

Start date: May 26, 2015
Phase: N/A
Study type: Interventional

Evaluation of the effectiveness of a sunscreen product by determining its Sun Protection Factor (SPF) on the skin of human subjects.

NCT ID: NCT02857725 Completed - Sunscreen Agents Clinical Trials

Sun Protection Factor (SPF) Assay

Start date: May 18, 2015
Phase: N/A
Study type: Interventional

Evaluation of the effectiveness of a sunscreen product by determining its Sun Protection Factor (SPF) on the skin of human subjects.

NCT ID: NCT02857478 Completed - Sunscreen Agents Clinical Trials

Supervised Outdoor-Use Test to Assess the Safety of a Sunscreen C-Spray on Sport Users

Start date: June 27, 2015
Phase: N/A
Study type: Interventional

The objective of this study was to assess the safety and appropriateness of a sunscreen product for use on sport users, under supervised outdoor-use conditions. The study was conducted under the supervision of a Board-Certified Dermatologist at an outdoor, chlorinated swimming pool facility.