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Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 42 days of participation
Awards & highlights
Study Summary
The purpose for this study is to assess the Safety and Efficacy of Daily Application for 4 weeks of DBI-001 Gel Versus Aqueous Gel in Subjects with Atopic Dermatitis
Eligible Conditions
- Atopic Dermatitis
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 42 days of participation
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~42 days of participation
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change From Baseline in Individual Signs and Symptoms of Atopic Dermatitis
Secondary outcome measures
Change in colony forming units
Change in colony forming units after using DBI-001 drug product or aqueous gel
Molecular diagnostic qPCR comparison of DBI-001 drug product with aqueous gel
+3 moreTrial Design
2Treatment groups
Active Control
Placebo Group
Group I: DBI-001 GelActive Control1 Intervention
DBI-001 Gel: Topical application of DBI-001 gel on skin affected with atopic dermatitis.
(This study is a within-subject bilateral controlled study)
Group II: Aqueous GelPlacebo Group1 Intervention
Aqueous Gel: Topical application of aqueous gel on skin affected with atopic dermatitis.
(This study is a within-subject bilateral controlled study)
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Who is running the clinical trial?
NorthsounddermUNKNOWN
ClearDermatologyandAestheticsCenterUNKNOWN
DermBiont, Inc.Lead Sponsor
11 Previous Clinical Trials
543 Total Patients Enrolled
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