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Skin Diseases clinical trials

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NCT ID: NCT04495036 Completed - Clinical trials for Dermatologic Disease

Acceptance of Telemedicine in Dermatology Patients, Physicians and Medical Staff

Start date: July 1, 2019
Phase:
Study type: Observational

This study is to investigate the current use and intention to use of teledermatology in Swiss dermatology patients, dermatologists, other physicians and medical staff.

NCT ID: NCT04493021 Completed - Pigmentation Clinical Trials

Evaluation of the Dermal Cooling System for the Enhanced Treatment of Benign Pigmented Lesions and Common Skin Conditions

Start date: July 7, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the Dermal Cooling System for lightening of benign pigmented lesions and to assess additional cosmetic benefits.

NCT ID: NCT04485676 Completed - Clinical trials for Skin Diseases, Infectious

Dalbavancin in Real Clinical Practice in Spain

REAL-DAL
Start date: July 15, 2020
Phase:
Study type: Observational

The aim of this study is to describe the real clinical use of Dalbavancin in Spain between January 2018 and December 2019.

NCT ID: NCT04472546 Completed - Healthy Clinical Trials

Use of the SpiderMass for in Vivo Analysis of the Skin in Five Chronic Inflammatory Dermatosis

Start date: December 13, 2019
Phase: N/A
Study type: Interventional

The physiological states of the skin are characterized by a certain homeostasis linked to the balance of the metabolic pathways. When these pathways are deregulated, the proteic, lipidic and metabolic is affected. It is thus possible to follow a change in the state of the skin by looking at change in the associated molecular profile. The PRISM laboratory (INSERM U1192) in Lille has developed an innovative system laser called SpiderMass composed of 4 parts: 1. A laser used for the micro-sampling of material in vivo, 2. A transport transfer line of the ablated particles, 3. A mass spectrometer that analyzes them in real time and generates the molecular profiles of the epidermis, 4. A data analysis procedure. The SpiderMass(TM) is of great interest for the study of the skin because it allows non-invasive vivo characterization, and therefore without biopsy or sample preparation. In addition, it will complement techniques already used in the research center such as FTIR spectroscopy. Indeed, in acne studies the FTIR allows to obtain only the Fatty Acid Triglycerid ratio while the SpiderMass permits to detail these lipid classes by each observed molecule on the surface of the skin and follow their evolution.

NCT ID: NCT04471896 Completed - Acne Clinical Trials

Joovvin' for Your Skin Health Study

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

Sixty day single arm trial examining self-report and remote dermatology assessment of cosmetic skin health after daily 10-20 minute sessions with an infrared light therapy device (the Joovv Mini)

NCT ID: NCT04456829 Completed - Skin Conditions Clinical Trials

Investigation of the Efficacies of a Resveratrol Formula on Improvement of Skin Conditions and Inflammatory Related Factors

Resveratrol
Start date: September 17, 2020
Phase: N/A
Study type: Interventional

To assess a resveratrol formula on improvement of skin conditions and inflammatory cytokines in blood

NCT ID: NCT04446923 Completed - Clinical trials for Surgical Site Infection

Surgical Hand Antisepsis With Propan-ol-1 60% Per Rubbing and Scrubbing

Start date: June 28, 2020
Phase: Phase 4
Study type: Interventional

The present study evaluates the effects of to compare bactericidal efficacy using the reference antiseptic product propan-ol-1 60% using the hand rub method versus hand scrub method in order to test if pass the standard european norm 12791.

NCT ID: NCT04445974 Completed - Quality of Life Clinical Trials

Testing a Body-functionality Intervention for Body Image in Individuals With Skin Conditions

Start date: December 15, 2020
Phase: N/A
Study type: Interventional

'Expand Your Horizons', a self-help writing intervention that seeks to train individuals to focus on what their body can do (functionality) rather than what it looks like (appearance), has produced promising results in improving body image. However, it has not been adapted and trialled in populations with conditions affecting skin appearance. This research therefore seeks to evaluate the potential for 'Expand Your Horizons' to (1) improve body image, as measured by body and functionality appreciation; and (2) improve skin-specific outcome, as measure by skin-shame, dermatology and quality of life, in a population with dermatological conditions, using a Randomised Control Trail.

NCT ID: NCT04404075 Completed - Atopic Dermatitis Clinical Trials

Skin Tracker: A Mobile Health App to Monitor Skin Disease Activity and Treatment Use

Start date: April 25, 2022
Phase:
Study type: Observational

Design and beta-test a research-oriented mobile health app to assess disease activity, quality of life, treatment patterns, adverse medication effects, and lifestyle factors in patients with atopic dermatitis.

NCT ID: NCT04378296 Completed - Skin Diseases Clinical Trials

Economic Evaluation in Teledermatology

TELEDERMA
Start date: April 1, 2021
Phase: N/A
Study type: Interventional

Introduction: Previous studies confirm that teledermatology allows the generation of a quick response from the specialist's consultation, reduction of unnecessary travels, early diagnosis and priority in the attention to the most urgent cases. Despite these advantages and that teledermatology has experienced exponential growth since its introduction approximately 16 years ago in Spain, in Andalusia, its use is still very limited. The objective of this project will be to carry out an analysis of the quality of life related to health, costs, cost-utility and informal care of teledermatology services in Primary Care compared to conventional monitoring carried out at the Hospital de Poniente. Methodology: A randomized, controlled, unmasked, inter-level clinical trial (Primary Care-Hospital de Poniente) and multicentre (all health centers attached to the Poniente Health District of Almería) will be carried out with a 6-month follow-up. Patients will be assigned to the teledermatology group (experimental) or the conventional monitoring group in the hospital (control). The patients included in the experimental group will be monitored asynchronously. Baseline characteristics, number of visits to the hospital, health-related quality of life, costs, informal care and satisfaction from the perspective of the Andalusian Public Health System and patients and their caregivers will be analyzed. The generic EuroQol-5D questionnaire (EQ-5D) will be administered to assess health-related quality of life and the SKINDEX-29 quality of life dermatological questionnaire. A cost-utility analysis will be performed to assess whether tele-dermatology is cost-effective in terms of additional cost for additional quality-adjusted life years (QALYs).