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Skin Diseases clinical trials

View clinical trials related to Skin Diseases.

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NCT ID: NCT02541721 Terminated - Clinical trials for Chronic Disease of Skin

Effectiveness and Tolerability of LabiaStick#01 in Subjects With Symptomatic Non-hypertrophic Chronic Vulvar Dermatoses

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

The current study aims to investigate the effectiveness in clinical symptomatic control and tolerability of LabiaStick#01 in women with symptomatic non-hypertrophic chronic vulvar dermatoses.

NCT ID: NCT02509650 Recruiting - Clinical trials for Very Rare Dermatologic Diseases

Identification of Mutations Responsible for Rare Familial Skin Diseases by Next Generation Sequencing

DERMA-SEQ
Start date: September 2015
Phase: N/A
Study type: Observational

The primary purpose of the protocol is to use next generation sequencing to identify pathogenic variants in genes involved in very rare skin diseases. The secondary purpose will be to study the genotype-phenotype correlation in order to re-evaluate the classification of these disorders. This work could help in the understanding of the physiopathology of very rare skin disorders.

NCT ID: NCT02500758 Enrolling by invitation - Clinical trials for Surgical Site Infection

Effectiveness of Preoperative Surgical Scrubbing Using Clorhexidine Digluconate and Parachlorometaxylenol (ECP)

ECP
Start date: June 2015
Phase: Phase 4
Study type: Interventional

Despite the wide variety of products and antiseptic agents, no agent is ideal for every situation. The investigators would like to evaluate the difference in reducing bacterial load, using 4% chlorhexidine digluconate and 3% parachlorometaxylenol after a preoperative surgical scrubbing.

NCT ID: NCT02499588 Recruiting - Ileostomy Clinical Trials

User Evaluation of the Peristomal Skin Condition in Ostomates Using ConvaTec Moldable Technology™

OSMOSE
Start date: June 2015
Phase: N/A
Study type: Observational

The primary aim of this study is to demonstrate the maintenance of healthy peri-stomal skin over a two month period in subjects who use ConvaTec Moldable Technology™ Skin Barriers as part of their standard protocol of care following surgery.

NCT ID: NCT02493283 Completed - Methemoglobinemia Clinical Trials

Pharmacokinetics and Distribution of Dapsone in Leucocytes After Single-dose and Multiple-dose Administration

Start date: September 2011
Phase: Phase 1
Study type: Interventional

The objectives of the study are - to evaluate pharmacokinetics, distribution in blood leucocytes, metabolism and methemoglobinemia after single-dose and repeated-dose administration of 100 mg of dapsone in healthy subjects genotyped for CYP2C9 and NAT2 - to evaluate serum through levels, distribution in blood leucocytes and methemoglobinemia after repeated-dose treatment with dapsone in patients with autoimmune bullous dermatoses before and after concomitant treatment with glucocorticoids

NCT ID: NCT02482896 Recruiting - Atherosclerosis Clinical Trials

The Lolland-Falster Health Study

LOFUS
Start date: February 2016
Phase: N/A
Study type: Observational

The study is a epidemiological, cross-sectional study in a mainly rural area of Denmark in Denmark. Life expectancy is shorter, morbidity is higher, and social problems more prevalent than in the urban areas of the country. The population study aims at examining complexities of environmental, hereditary, lifestyle, and social factors as determinants and predisposing factors for morbidity, health, and quality of life. The study will cover physical, mental, and social dimensions and examine family patterns and subgroups. The study will provide baseline information for later follow-up.

NCT ID: NCT02477514 Completed - Clinical trials for Skin Diseases, Bacterial

A Study to Evaluate the Effects of Tedizolid Phosphate on the Pharmacokinetics and Safety of Midazolam and Rosuvastatin (MK-1986-004)

Start date: June 2015
Phase: Phase 1
Study type: Interventional

The purpose of this study is to assess the effect of steady-state tedizolid phosphate on the single-dose pharmacokinetics of midazolam and rosuvastatin in healthy, adult participants.

NCT ID: NCT02471352 Recruiting - Healthy Volunteers Clinical Trials

Studies of Dermatologic Diseases Biospecimen Acquisition Protocol

Start date: June 19, 2015
Phase:
Study type: Observational

Background: - Skin disease can have many causes. It can have widespread consequences, and in rare cases can lead to death. Researchers want to determine the causes of various types of skin diseases and find a way to treat them. Objectives: - To determine the causes of various skin diseases and find ways to treat them. Eligibility: - People ages 2 and older who have: - A skin disease or at risk of developing a skin disease OR - A family member of persons with a skin disease - Healthy volunteers ages 2 and older Design: - Participants will be screened under a separate protocol. - Participants may take a survey about how their skin condition affects their quality of life. - Participants will have a medical history and a physical exam including a detailed skin exam. Pictures will be taken of their skin to document any skin disease. - Participants will have specimens collected. This may include: - Several teaspoons of blood taken at each visit - Stool samples - Nail and body fluid (like saliva) samples - Cheek swabs. The inside of the cheek will be scraped for about a minute in each direction to collect cells. - Collection of skin samples with: - A swab (like a Q-tip) - Gently scraping skin to remove the outer layers of cells - Applying and removing 1-inch pieces of tape - Participants may have up to 4 skin biopsies in 12 months, with 4 separate biopsies taken each time. - An area of skin will be numbed with an injection. - A piece of skin the size of a pencil eraser will be removed using a small instrument. - A flat scar usually develops at the biopsy site.

NCT ID: NCT02465476 Completed - Skin Disease Clinical Trials

Rationalization of the Treatment Pathway of Patient Suffering From Rare Skin Disease With Telemedicine

Telemalrares
Start date: January 6, 2015
Phase: N/A
Study type: Interventional

The investigators want to demonstrate that a new organization with telemedicine could rationalize the treatment pathway of patient suffering from rare skin disease. A diagnosis and a personalised treatment pathway could be performed before the consultation in the hospital.

NCT ID: NCT02443272 Completed - Clinical trials for Abscess of Skin and/or Subcutaneous Tissue

Comparison of Loop Drainage Versus Incision and Drainage for Abscesses in Children

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

The purpose of this study is to compare abscess drainage utilizing the vessel loop technique in children to the standard incision and drainage technique with the endpoint to determine if rates of treatment failure are non-inferior.