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Skin Care clinical trials

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NCT ID: NCT02792595 Completed - Skin Care Clinical Trials

In Vivo Sun Protection Factor Determination

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

The study aims to determine the Sun Protection Factor (SPF) of 8 cosmetic products in vivo on the back of human participants, according to the International Standard Sun Protection Test method by using a sun simulator.

NCT ID: NCT02603029 Completed - Wrinkles Clinical Trials

Influence of of Cream With the Silver Fir Wood Extract (Belinal) on Skin

Start date: March 2015
Phase: N/A
Study type: Interventional

Objective of the study is to determine the influence of the cream with Silver fir wood (Abies alba) extract (Belinal) on the skin parameters and functions in comparison to the placebo cream. 10 healthy female subjects will use the test cream on one half and placebo cream on the other half of the face and of the gluteal part twice a day for 12 weeks. Various face skin parameters will be evaluated before the cream use (the baseline), after 6 and after 12 weeks of the cream use. To evaluate the photoprotective potential of Belinal the minimal erythema dose (MED) will be determined before (the baseline) and after 12 weeks of the cream use at the gluteal area.

NCT ID: NCT02403999 Completed - Skin Care Clinical Trials

A Tolerability Assessment Study of Three Wash Products in Infants

Start date: March 1, 2015
Phase: N/A
Study type: Interventional

This will be a single centre, evaluator blind, randomized, parallel group, stratified, two week study in healthy participants. The clinical study is designed to provide reassurance that the formulations developed for children and babies with mild to moderately dry skin and for children whose skin is prone to atopic dermatitis (eczema) are well tolerated in the target population, babies and young children with dry skin.

NCT ID: NCT02106403 Completed - Skin Care Clinical Trials

A Study to Evaluate the Cooling Sensation and Consumer Liking of a Skin Disinfectant Spray

Start date: May 2014
Phase: N/A
Study type: Interventional

The objective of this randomised, examiner and subject blinded study is to evaluate and compare cooling performance and overall consumer liking of the prototype formulation with the currently marketed wound spray and negative control in subjects with experimental wounds. For each subject, three superficial wounds will be induced on two volar forearms, by sequential tape strippings until a glistening layer is visualized. After wounding, a randomised test product will be sprayed twice on test site, and the subject will be asked to complete a questionnaire evaluating product cooling performance and overall liking.