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Tencel Therapeutic Garments for Atopic Dermatitis
N/A
Waitlist Available
Led By Annie Grossberg, MD
Research Sponsored by Johns Hopkins University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be younger than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline (at study initiation), 1 month, 2 months, and 3 months
Awards & highlights
Study Summary
Tencel vs. Standard Cotton Therapeutic Garments as an Adjunct Treatment for Moderate to Severe Atopic Dermatitis in Children
Eligible Conditions
- Atopic Dermatitis
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline (at study initiation), 1 month, 2 months, and 3 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline (at study initiation), 1 month, 2 months, and 3 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in Atopic Dermatitis Severity score as assessed by Eczema Area and Severity Index (EASI) score
Dermatitis, Atopic
Secondary outcome measures
Change in patient-reported pruritus as assessed by ItchyQoL
Change in patient-reported quality of life as assessed by Children's Dermatology Life Quality Index (CDQLI)
Change in patient-reported quality of life as assessed by Infant's Dermatitis Quality of Life Index (IDQoL)
+1 moreTrial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: Tencel Therapeutic GarmentsExperimental Treatment1 Intervention
Children in this group will wear Tencel Therapeutic Garments
Group II: Cotton Therapeutic GarmentsPlacebo Group1 Intervention
Children in this group will wear Cotton Therapeutic Garments
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Who is running the clinical trial?
Johns Hopkins UniversityLead Sponsor
2,252 Previous Clinical Trials
14,817,664 Total Patients Enrolled
AD RescueWearOTHER
Annie Grossberg, MDPrincipal InvestigatorJohns Hopkins University
Frequently Asked Questions
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