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Skin Diseases clinical trials

View clinical trials related to Skin Diseases.

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NCT ID: NCT04775316 Terminated - Wounds and Injuries Clinical Trials

Prospective, International, Multicenter, Observational Study to Evaluate the Clinical Performance and Safety of a Silicone-coated Transparent Postoperative Dressing

Start date: September 1, 2021
Phase:
Study type: Observational

Although, a huge number of acute wounds is treated successfully every year, Health Care Professionals (HCPs) are facing more and more problems when treating skin damages or surgical incisions: The number of patients with fragile and/or sensitive skin is highly increasing. Such patients are having a skin integrity issue, meaning the skin is vulnerable to injury, often damaged, or unable to heal. The investigational medical devices (IMDs) of the planned clinical evaluation, Leukomed® T skin sensitive and Leukomed® T plus skin sensitive have been developed for treatment of acute wounds on patients with fragile or sensitive skin to provide a reliable but skin-friendly fixation and wound care option. The primary purpose of this clinical study is the evaluation of clinical performance to stay in place up to seven days and the safety of both dressings. Further, data on wearing comfort, product handling, pain during removal and quality of life are considered as secondary outcomes. The products will be used as part of routine wound care within the scope of their intended purpose without any additional invasive or burdensome examination.

NCT ID: NCT04763512 Recruiting - Atopic Dermatitis Clinical Trials

Clinical Study of Partially Hydrolysed Protein Infant Formula on Trans-epidermal Water Loss (TEWL)

Start date: June 6, 2021
Phase: N/A
Study type: Interventional

This is a single-centre, prospective, randomized, open-label, controlled trial of 200 infants 42±7 days of age. Subjects will be randomized to one of two open label feeding intervention group: - Intact Cow's Milk Protein Formula Group (CMFG) (n = 100) or - Partially Hydrolysed Whey Formula Group (pHFG) (n = 100).

NCT ID: NCT04760314 Completed - Dermatitis, Atopic Clinical Trials

A Study of Lebrikizumab (LY3650150) in Combination With Topical Corticosteroids in Japanese Participants With Moderate-to-Severe Atopic Dermatitis

ADhere-J
Start date: March 10, 2021
Phase: Phase 3
Study type: Interventional

The main purpose of this study is to evaluate the efficacy and safety of lebrikizumab in combination with a topical corticosteroids in Japanese participants with atopic dermatitis.

NCT ID: NCT04750161 Recruiting - Atopic Dermatitis Clinical Trials

The Role Of Neutrophil Proteases As Global Regulators Of Il-1 Family Cytokine Activity In Skin Disorders

NEUTROPRO
Start date: March 2, 2021
Phase:
Study type: Observational

Pro-inflammatory cytokines are critically important drivers of inflammatory and autoimmune diseases and cytokine-targeted biologics have been transformative in the treatment of several inflammatory and autoimmune diseases. As the diversity of approved cytokine-targeted biologic therapies grows, it will become increasingly important to stratify patients on the basis of specific genetic or disease biomarker phenotypes to ensure that patients receive the appropriate cytokine-targeted biologic, at the appropriate dose, and at the appropriate time. This project aims to explore patterns of pro-inflammatory cytokine/chemokine expression within normal versus (i) psoriatic, (ii) eczematic, (iii) ichthyotic human skin, as well as in human and mouse models of skin inflammation, with the objective of identifying cytokine response profiles ('cytokine fingerprints') that will provide a molecular basis for (a) the stratification of patients into disease subtypes that (b) enable cytokine-directed biologics to be targeted towards patients that are most likely to benefit from them. The investigators anticipate that 'cytokine fingerprinting' will aid in the selection of the most appropriate biologics in patients that are most likely to benefit from such therapies.

NCT ID: NCT04739228 Completed - Clinical trials for Psychological Distress

Effects of Guided Written Disclosure Protocol on Psychological Distress and Positive Functioning in Persons With Skin Diseases: a Randomized-controlled Trial

Start date: July 1, 2017
Phase: N/A
Study type: Interventional

We conducted a randomized-controlled trial of Guided Written Disclosure Protocol for dermatological patients with the aim of reducing psychological distress, expressive suppression, and skin-related symptoms, and improving spiritual well-being, cognitive reappraisal, and sense of coherence.

NCT ID: NCT04733872 Completed - Skin Condition Clinical Trials

Using Vegetable and Berry Products Can Improve Skin Conditions

Start date: October 1, 2017
Phase: N/A
Study type: Interventional

Hypothesis: vegetable and berry products for 8 weeks can improve skin condition

NCT ID: NCT04733859 Completed - Skin Condition Clinical Trials

Using Red Djulis Products Can Improve Skin Conditions

Start date: October 1, 2017
Phase: N/A
Study type: Interventional

Hypothesis: Using red djulis products can improve skin conditions

NCT ID: NCT04731389 Completed - Acne Clinical Trials

Digital Strategies for Patients With Chronic Dermatosis With Pruritus / Skin Picking Disorder

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

Almost 35% of patients treated to dermatosis have some psychiatric disorder. The aim of this study is to evaluate the prevalence and severity of skin picking disorder and other dermatosis, and also test the efficacy of an online-delivered cognitive-behavioral therapy to improve skin picking disorder severity.

NCT ID: NCT04725292 Completed - Skin Diseases Clinical Trials

Rare Benign Lesion of Peins

Start date: January 12, 2021
Phase:
Study type: Observational

PEKMB was first named and described by Lortat-Jacob & Civatte in 1961 and by Bart & Kopf later. This rare condition is mostly reported in elderly males. The keratotic scales is usually micaceous and resembles psoriasis. Most patients are above 50 years of age and are circumcised later in life, but also reported in younger age group. This mica like scales contains keratin which gets dissolved in 10% potassium hydroxide solution. Disease progression may lead to phimosis. Differential diagnosis of this disease entity include moniliasis, wart, psoriasis ,penile horn, circinate balanitis, erythroplasia of Queyrat, squamous cell epithelioma and verrucous carcinoma. It is primarily a benign entity, it is capable of invasiveness. Bart and Kopf considered it to be in intermediate stage between benign hyperplasia and squamous cell carcinoma. However, the histological spectrum can range from hypertrophic-hyperplastic penile dystrophy to verrucous carcinoma. Fibro sarcoma has been reported developing in a same patient. Etiology is unclear. Despite search for a viral agent, Human Papilloma Virus (HPV) has not been demonstrated and its role in pathogenesis or its transformation to verrucous carcinoma has been proved. The treatment of PEKMB should be conservative when there is no histological evidence of malignancy. All such patients should be followed up. Treatment choices include potent topical steroids, topical 5% 5-flurouracil cream1, 2, cryotherapy, radiotherapy and shaving biopsy plus electro coagulation. When frank malignancy is observed, excision with wide margin is the rule.

NCT ID: NCT04709588 Completed - Skin Condition Clinical Trials

Hydrolyzed Collagen Combined With Djulis and Green Caviar Improve Skin Condition

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

Collagen combined with djulis and green caviar improve skin condition