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Active clinical trials for "Dermatitis Herpetiformis"

Results 1-5 of 5

Background of Different Phenotypes of Coeliac Disease

Celiac DiseaseDermatitis Herpetiformis

The main purpose of this study is to investigate genetic, serological, immunological and microbiata diversities between different coeliac disease phenotypes and to discover applicable prognostic markers for specific phenotypes.

Recruiting5 enrollment criteria

Use of Dapsone Gel, 5% for Treating Dermatitis Herpetiformis

Dermatitis Herpetiformis

The primary objective of this study is to evaluate the efficacy of dapsone gel, 5% in the treatment of dermatitis herpetiformis. The primary efficacy end point will be the proportion of patients achieving success based on mean % reduction from baseline in total lesion counts at week six. Success for lesion reduction will be defined as statistically greater mean percent reductions at week six in the dapsone gel-treated extremity compared with the control extremity of each patient.

Terminated8 enrollment criteria

Dermatitis Herpetiformis Refractory to Gluten Free Diet

Dermatitis Herpetiformis

The main purpose of the study is to find out the natural course of refractory dermatitis herpetiformis and the development of possible complications the strictness of gluten-free diet treatment in refractory dermatitis herpetiformis

Enrolling by invitation10 enrollment criteria

Study of Enzyme Supplements to Treat Celiac Disease

Celiac DiseaseDermatitis Herpetiformis

The purpose of this study is to examine whether a cocktail of two common food-grade enzyme supplements leads to decrease of serum activity markers in celiac disease patients insufficiently treated by previous gluten exclusion.

Completed8 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
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