Yulex Glove

Sex: Female, Male

Region of Enrollment

The primary study outcome will be an assessment for sensitization to Yulex as determined by serological assay for Guayule-specific IgE antibodies. The development of a detectable IgE immune response will be considered a positive study.

Sensitization to Yulex

A secondary study outcome is the development of an immune response to Yulex using a human IgG anti-Guayule immunoassay. The development of a detectable IgG immune response will be considered a positive study.

Immune Response to Yulex

Eligibility Assessment

Intervention Allocation

Eric Levey, M.D.

Spina Bifida

Latex Allergy

Study participants will be asked to wear Yulex gloves for routine bowel and bladder care (~30 minutes per day) over a 3 month period.

Yulex gloves

Hugo W. Moser Research Institute at Kennedy Krieger Inc.

Yulex Glove Prospective Study in Spina Bifida

Yulex Glove Prospective Study

Charles Curry

Research assistant/co-investigator

Hugo W. Moser Research Institute at Kennedy Krieger, Inc.

Johns Hopkins University

Parthenium Dermatitis

azathioprine and corticosteroids for Parthenium dermatitis

Department of Dermatology, AIIMS

Azathioprine Versus Corticosteroids in Parthenium Dermatitis

Azathioprine Versus Corticosteroids for the Treatment of Parthenium Dermatitis

All India Institute of Medical Sciences, New Delhi

parthenium incanum

hypersensitivity

parthenium

parthenium incanum/hypersensitivity

Yulex Glove Prospective Study in Spina Bifida

Azathioprine Versus Corticosteroids in Parthenium Dermatitis

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