CeraVe Cream Compared to Desitin Paste for Treating Diaper Dermatitis in Infants
Status: | Terminated |
---|---|
Conditions: | Dermatology |
Therapuetic Areas: | Dermatology / Plastic Surgery |
Healthy: | No |
Age Range: | Any |
Updated: | 4/17/2018 |
Start Date: | December 2014 |
End Date: | July 2016 |
Randomized, Double-Blind, Parallel Group, Non-Inferiority Clinical Trial of CeraVe Baby Diaper Rash Cream Compared to Desitin Maximum Strength Original Paste for Management of Diaper Dermatitis in Infants
This is a single-center, 1:1 randomized, double-blind, parallel-group, non-inferiority
controlled trial to demonstrate non-inferiority of CeraVe Baby Diaper Rash Cream compared to
Desitin Maximum Strength Original Paste when administered to children with diaper dermatitis
who are between 3 months to 18 months of age. Parents/caregivers of subjects in both groups
will administer the product with each diaper change throughout the course of the study
period. Product can be applied liberally as needed. Diapers and skin cleansing interventions
will stay constant throughout the treatment period. Subjects will be assessed by the study
doctor, parent/caregiver will be asked about any adverse effects. Parent/caregivers will also
be asked to complete a daily diary that asks about changes in their baby's diaper dermatitis,
a Visual Analogue Scale severity assessment of their baby's diaper dermatitis, and
observations related to product use and the baby's comfort level. Parents/caregivers will
also be given a questionnaire rating the use of the study products.
controlled trial to demonstrate non-inferiority of CeraVe Baby Diaper Rash Cream compared to
Desitin Maximum Strength Original Paste when administered to children with diaper dermatitis
who are between 3 months to 18 months of age. Parents/caregivers of subjects in both groups
will administer the product with each diaper change throughout the course of the study
period. Product can be applied liberally as needed. Diapers and skin cleansing interventions
will stay constant throughout the treatment period. Subjects will be assessed by the study
doctor, parent/caregiver will be asked about any adverse effects. Parent/caregivers will also
be asked to complete a daily diary that asks about changes in their baby's diaper dermatitis,
a Visual Analogue Scale severity assessment of their baby's diaper dermatitis, and
observations related to product use and the baby's comfort level. Parents/caregivers will
also be given a questionnaire rating the use of the study products.
Visit 1 - Screening and Baseline Visit (Day 0) Subjects will be evaluated for study
eligibility using inclusion and exclusion criteria. The study doctor will assess diaper
dermatitis for inclusion and exclusion criteria and to verify mild to moderate severity. Once
study eligibility has been confirmed, parental/guardian consent will be obtained. No washout
period is necessary for this study.
Location of clinically apparent involved area will be shaded by hand onto diagram by the
research personnel. Study products will be dispensed to parent/caregiver, along with
instructions for administration. Parent/caregivers will also be asked to complete a daily
diary that asks about changes in their baby's diaper dermatitis, a Visual Analogue Scale
severity assessment of their baby's diaper dermatitis, and observations related to product
use and the baby's comfort level. Parents/caregivers will be asked to complete the daily
diary for each day of the study.
Visit 2 (Day 7) Subjects will again be assessed by the study doctor. Parent/caregiver will be
asked about any adverse effects in last 7 days.
Visit 3 - End of study (Day 14) Subjects will again be assessed by the study doctor. Daily
diaries and product will be collected at this time. Parent/caregiver will be asked about any
adverse effects in last 7 days. Parents/caregivers will also be given a questionnaire rating
the use of the study products.
eligibility using inclusion and exclusion criteria. The study doctor will assess diaper
dermatitis for inclusion and exclusion criteria and to verify mild to moderate severity. Once
study eligibility has been confirmed, parental/guardian consent will be obtained. No washout
period is necessary for this study.
Location of clinically apparent involved area will be shaded by hand onto diagram by the
research personnel. Study products will be dispensed to parent/caregiver, along with
instructions for administration. Parent/caregivers will also be asked to complete a daily
diary that asks about changes in their baby's diaper dermatitis, a Visual Analogue Scale
severity assessment of their baby's diaper dermatitis, and observations related to product
use and the baby's comfort level. Parents/caregivers will be asked to complete the daily
diary for each day of the study.
Visit 2 (Day 7) Subjects will again be assessed by the study doctor. Parent/caregiver will be
asked about any adverse effects in last 7 days.
Visit 3 - End of study (Day 14) Subjects will again be assessed by the study doctor. Daily
diaries and product will be collected at this time. Parent/caregiver will be asked about any
adverse effects in last 7 days. Parents/caregivers will also be given a questionnaire rating
the use of the study products.
Inclusion Criteria:
- Healthy children (except for diaper dermatitis) between 3 and 18 months of age
- Wearing diapers 24 hours per day
- Clinical irritant diaper dermatitis
- Received a Diaper Dermatitis severity score of 1.0 to 2.0 by investigator at screening
visit (mild-moderate severity)
- Parent/caregiver will not change type or brand of diaper during the study, although
the diaper type will be recorded
- No alteration of current product usage for creams, lotions, ointments, powders, soap,
laundry detergents, and fabric softeners
- A parent or guardian of minors must sign the approved Institutional Review Board
consent form prior to the conduct of any study-related procedures
Exclusion Criteria:
- Illness within past 4 days before study enrollment or any medical condition that may
affect risk of study participation
- Does not wear diapers 24 hours per day or currently being toilet trained
- Active diagnosis or history of dermatological conditions other than diaper rash that
may affect study
- Concomitant use of medications that may affect study (e.g., antifungal, topical
steroid, or topical calcineurin inhibitor)
- Previous allergic reaction or known sensitivity to ingredients in study agents
We found this trial at
3
sites
225 E Chicago Ave
Chicago, Illinois 60611
Chicago, Illinois 60611
(312) 227-4000
Ann & Robert H. Lurie Children's Hospital of Chicago Ann & Robert H. Lurie Children
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