Status:

COMPLETED

In-home Use Test of the New Modified Diprobase Formulation to Assess the Safety and Tolerability in Infants and Children Under Physician's Control

Lead Sponsor:

Bayer

Conditions:

Atopic Dermatitis

Eligibility:

All Genders

6-48 years

Phase:

NA

Brief Summary

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).

Eligibility Criteria

Inclusion

  • 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

Exclusion

    Key Trial Info

    Start Date :

    September 26 2018

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ACTUAL

    End Date :

    August 2 2019

    Estimated Enrollment :

    40 Patients enrolled

    Trial Details

    Trial ID

    NCT03441568

    Start Date

    September 26 2018

    End Date

    August 2 2019

    Last Update

    July 24 2020

    Active Locations (1)

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    West Timperley Medical Centre

    Altrincham, United Kingdom, WA14 5PF

    In-home Use Test of the New Modified Diprobase Formulation to Assess the Safety and Tolerability in Infants and Children Under Physician's Control | DecenTrialz