Atopic Dermatitis Clinical Trial
Official title:
In-home Use Test of the New Modified Diprobase® Formulation to Assess the Safety and Tolerability in Infants and Children Under Physician's Control
Verified date | July 2020 |
Source | Bayer |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
To investigate the safety and tolerability of the modified Diprobase formulation over 14 days in infants and children with a history of Atopic Dermatitis (AD).
Status | Completed |
Enrollment | 40 |
Est. completion date | August 2, 2019 |
Est. primary completion date | August 2, 2019 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 6 Months to 48 Months |
Eligibility |
- Children with normal or dry skin and a history of mild to moderate AD, but without any
signs or symptoms within the last month prior to enrollment - Skin type I - VI according to Fitzpatrick skin classification - Aged 6 months to 48 months |
Country | Name | City | State |
---|---|---|---|
United Kingdom | West Timperley Medical Centre | Altrincham |
Lead Sponsor | Collaborator |
---|---|
Bayer |
United Kingdom,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Number of participants with adverse event (AE) | Up to 14 days | ||
Primary | Severity of adverse event | The intensity of an AE is classified according to the following categories: Mild Moderate Severe |
Up to 14 days |
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