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Xerosis clinical trials

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NCT ID: NCT04245319 Recruiting - Depression Clinical Trials

Combined Effect of Acitretin and Narrow Band Ultraviolet B on Vitiligo Repigmentation

Start date: January 1, 2020
Phase: N/A
Study type: Interventional

Since abnormal keratinocyte (KC) proliferation and differentiation as well as defective E cadherin expression were reported in vitiligo lesions, the investigators set to study the potential efficacy of combining Retinoids, which are known to improve KC proliferation and differentiation and increase the expression of adhesion molecules, with narrowband UVB in the treatment of vitiligo.

NCT ID: NCT04181177 Completed - Xerosis Clinical Trials

Efficacy Study of Cosmetic Product on Xerosis Induced by Systemic Anticancer Treatments

Start date: February 19, 2019
Phase:
Study type: Observational

Xerosis is one of the most common adverse events in patients treated with new cancer therapies and chemotherapies, such as multi-kinase inhibitors and more specifically, immunological checkpoint inhibitors used in the treatment of several cancers. Xerosis appears as a result of a deterioration of the stratum corneum which results in a reduction of the hydric power of the skin. It reaches the trunk and limbs, with an incidence of 4-35%, and gradually disappears after the end of treatment. Preventive targeted educational action is essential before initiation of cancer treatment. Once the xerosis is installed, the management is based on the use of emollients to contribute to the hydric correction of the skin. In the case of inflammation or associated infection, the administration of topical corticosteroids and / or local or oral antibiotic therapy is prescribed. The aim of this study is to evaluate the efficacy of the cosmetic product (balm) on the improvement of xerosis induced by systemic anticancer treatments, in participants receiving targeted educational action compared to a control group. Clinical, biological and biometrological assessments will be performed to characterized the effects in both induced xerosis and associated signs and symptoms. Each group will include 40 participants.

NCT ID: NCT03497130 Completed - Itching Clinical Trials

The Role of Skin Care Regimen in Skin Health

Start date: April 10, 2018
Phase: N/A
Study type: Interventional

This research is being done to evaluate the role of a regular skin care regimen comprising of a mild soap and moisturizer in improving dry skin and overall skin health. In this study, the investigators hope to learn the importance of regular skin care regimen in improving dry skin and overall skin health.

NCT ID: NCT03093597 Completed - Xerosis Cutis Clinical Trials

Skin Barrier Biophysical Properties and Clinical Appearance After Moisturizer in Dry Skin

Start date: March 27, 2017
Phase: N/A
Study type: Interventional

The purpose of the study is to compare the changes in the appearance of dry skin after the use various moisturizers: white petrolatum ointment, coconut oil, jojoba oil, and almond oil in patients with dry skin.

NCT ID: NCT02429206 Completed - Xerosis Clinical Trials

Safety and Efficacy of SQIN™ on Xerosis in Adults With Mobility Problems and Paralysis

Start date: April 2015
Phase: Phase 2/Phase 3
Study type: Interventional

In the general population, xerosis is often caused by external factors such as seasonal changes. In that case, the best way to relieve dry skin is to use a standard moisturizer. However, for those suffering of mobility problems due to age or paralysis (e.g., spinal cord injury, multiple sclerosis, Parkinson's, etc), xerosis is often severe and chronic because of the multiple causes (endogenous rather than exogenous ones) underlying such mobility impairment-related skin problems. This study is a double-blind, randomized study with positive control (active comparator) to assess the safety and efficacy of SQIN with CanSATs (Co-Activation of Natural Synergistically Acting Target-receptorS) technology on dry skin in patients suffering of paralysis.