Completed

SpongioticMolecular and Cellular Characterization of Spongiotic Dermatitis

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What is being collected

Data Collection

Collected from today forward - Prospective
Who is being recruted

Dermatitis+11

+ Dermatitis, Atopic

+ Dermatitis, Contact

From 18 to 55 Years
See all eligibility criteria
How is the trial designed

Case-Control

Comparing exposures between individuals with and without disease in order to identify potential risk factors.
Observational
Study Start: September 2006
See protocol details

Summary

Principal SponsorUniversity of California, Davis
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: September 1, 2006

Actual date on which the first participant was enrolled.

Spongiotic dermatitis is the histopathologic diagnosis commonly issued by dermatopathologists that encompasses atopic dermatitis, contact dermatitis, and other forms of eczematous dermatitis. Atopic dermatitis is a chronic, relapsing inflammatory disease characterized by pruritic, scaly, red, eczematous skin lesions, and a personal or family history of atopy. Patients affected by atopic dermatitis experience significant morbidity from extreme pruritus, recurrent cutaneous infections, and extensive and/or disfiguring skin lesions. Allergic contact dermatitis typically manifests as pruritus and vesicular or eczematous lesions associated with direct exposure to environmental haptenic allergens. The specific aims of this research are: 1. Identification of genes differentially expressed in atopic dermatitis, contact dermatitis, and psoriasis by microarray analyses. 2. Confirmation of protein expression profiles in atopic and contact dermatitis, and psoriasis by immunohistochemical analyses. 3. Identification of disease-specific potential diagnostic markers in plasma and PBMC. The information obtained will assist in development of diagnostic methods for differentiation of the types of spongiotic dermatitis. This study also has the potential to lead to the dissection of pathologic pathways involved in these diseases and development of novel therapeutic agents.

Official TitleMolecular and Cellular Characterization of Spongiotic Dermatitis
NCT00371163
Principal SponsorUniversity of California, Davis
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

31 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Case-Control

These studies compare people who have a disease (cases) with those who don't (controls). The goal is to look back at previous exposures or risk factors to identify what might have contributed to the disease.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 18 to 55 Years

Range of ages for which participants are eligible to join.

Healthy volunteers allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

DermatitisDermatitis, AtopicDermatitis, ContactHypersensitivityHypersensitivity, ImmediateImmune System DiseasesCongenital, Hereditary, and Neonatal Diseases and AbnormalitiesPsoriasisSkin DiseasesSkin Diseases, GeneticSkin and Connective Tissue DiseasesSkin Diseases, EczematousSkin Diseases, PapulosquamousGenetic Diseases, Inborn

Criteria

Inclusion Criteria: 1. Atopic Dermatitis: Subjects will be identified based on the Hanifin criteria of atopic dermatitis. Subjects will be adults with a history of atopic dermatitis since childhood, who continue to have symptoms and signs of atopic dermatitis. They must have active lesions and should not be on systemic therapy. 2. Contact Dermatitis: Subjects will be adults with history of contact dermatitis to common allergens. They will undergo patch testing to common allergens and the sites of positive reactions will be considered as lesional skin. 3. Psoriasis: Subjects will be adults with chronic disease, who have active skin lesions with a characteristic morphology. Subjects will be asked to discontinue topical medications at least to parts of the skin where biopsies will be taken, one week prior to biopsy. \- Exclusion Criteria: * Patients on systemic treatment of their skin diseases within the past one month. * A history of significant neurologic, hepatic, renal, endocrine, cardiovascular, gastrointestinal, pulmonary, or metabolic diseases. * Abnormal hepatic function or renal function (creatinine or BUN is \> 1.2 times the upper level of the normal range for the laboratory where the testing is done). * Abnormal blood counts (WBC \< 4 x 103/mm3; platelet \< 100 x 103/mm3; hemoglobin \< 11g/dl). * History of alcohol or drug abuse. * Known hepatitis or HIV. * Pregnant women (as determined by serum pregnancy test). * Significant allergic or adverse reaction to local anesthetics. * Blood clotting disorder. * Faintness or vasovagal reaction with blood draws or procedures.

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Study Objectives

Study Objectives

Primary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

UC Davis Department of Dermatology

Sacramento, United StatesOpen UC Davis Department of Dermatology in Google Maps
CompletedOne Study Center