search

Active clinical trials for "Erythema"

Results 111-112 of 112

Affect of Dose Rate on UVR Induced Skin Erythema

Erythema

Purpose of study: Evaluation of the affect of dose rate on UVR induced skin erythema. Study design: A single-center, prospective, randomized, crossover, open study. Number of patients: 20-40 Patient population: Healthy volunteers Control: Different sites on patients body Procedure duration: Total 3-5 hours (4 visits) Duration of follow up: 4 days Duration of study: Up to 6 months Primary objectives: To examine the difference in erythemal response as a function of dose rate, and to assess the total amount of energy that is theoretically transmitted through a sunscreen within the range of SPF 2-10.

Unknown status8 enrollment criteria

Observational Study of the Genetic Architecture of Neutrophil-Mediated Inflammatory Skin Diseases...

Other Specified Inflammatory Disorders of Skin or Subcutaneous TissuePyoderma Gangrenosum26 more

This study investigates the genetic architecture of Neutrophil-Mediated Inflammatory Skin Diseases. After collecting informed consent, all patients' clinical phenotype is graded at inclusion with a detailed case report form and a discovery cohort formed based on the certainty of diagnosis. The DNA of patients in the discovery cohort is analyzed by whole exome sequencing which identifies all protein-coding genetic variants. Subsequently, statistical burden tests are going to identify enrichment of rare coding genetic variants in patients affected by Neutrophil-Mediated Inflammatory Skin Diseases. The ultimate goal is to reveal the responsible gene(s) that may then be targets for clinical intervention.

Unknown status3 enrollment criteria
1...1112

Need Help? Contact our team!


We'll reach out to this number within 24 hrs