Evaluation of the Safety and Performance of LiNiDERM® in the Prevention of Infant Diaper Rash

April 2, 2019 updated by: Laboratoires Gilbert

Evaluation of the Safety and Performance of LiNiDERM® in the Prevention of Infant Diaper Rash: a Randomized Clinical Trial

Result of immaturity of the skin and factors promoting maceration and mechanical interactions, Irritant diaper dermatitis (IDD) can manifest as early as the third week of life. IDD is a form of contact dermatitis and is the most common inflammatory dermatitis of the diaper area infants. This dermatitis is very common amongst first year of life.

The IDD is characterized by erythema on the convex surfaces with the skin folds spared (W-shaped erythema) and it can cause considerable pain and stress for infants and can be troublesome for their caregivers.

The development of IDD is multifactorial. The critical step in the development of IDD is the occlusion of the skin under the diaper. The skin in the diaper area is predisposed to irritation by the presence of urine, stool, friction on the skin and presence of a high skin pH (potential Hydrogen).

At the cellular level, there is a gradual disorganization of the lipid layers and later an attack of keratinocytes. Clinically, maceration is followed by an inflammatory reaction.

Hence, infrequent diaper changes create overhydration and maceration of the stratum corneum, which makes the skin more sensitive to friction; this may interfere with the protective barrier function, allowing for the exposure of the lower layers to irritants (mechanical, chemical and infectious).

The removal of maceration and the reduction of friction are the key to prevention. But it is recommended to respect preventive measures, in order to preserve the normal skin condition over the long term. Special care procedures are required to ensure healthy development and to protect the skin from irritation and inflammation, as well as a sense of well-being. Although use of appropriately formulated cleansers and emollients can help maintain the epidermal skin barrier in the diaper region, good hygiene and adequate protection are necessary to prevent skin barrier breakdown, rash and infection. The prevention of IDD includes frequent diaper changing, parent education and cleaning.

LiNiRASH is a monocentric, prospective, randomized, comparator controlled study conducted under paediatric control. 132 infants will be followed in this study for 4 weeks during which their parents will use a specific cleaning method: water and cotton pads or wipes or liniment. The objective of this study is to compare the performance and safety of this 3 cleaning methods on the prevention of infant diaper rash.

Study Overview

Status

Completed

Conditions

Study Type

Interventional

Enrollment (Actual)

133

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Gdańsk, Poland
        • Dermscan

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

3 months to 3 years (Child)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Aged 3 - 36 months, in good health, born at term or up to 1 month before term,
  • A skin phototype I- III according to Fitzpatrick scale,
  • Wearing diapers daily with at least 2 changes per day and a night port,
  • For whom parents have given their written informed consent regarding its participation in this clinical investigation.

Exclusion Criteria:

  • Wearing washable or pull-on diapers,
  • Presenting a diaper rash (in progress),
  • Presenting a cutaneous pathology known,
  • Treated actually by phototherapy,
  • Presenting a cow's milk protein allergy,
  • Under medical treatment which may interfere with studied products and/ or skin in the 4-weeks prior to enrolment.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Liniderm

Oleocalcareous liniment Liniderm:

The product will be applied on the diaper area by parents/ caregivers at each diaper change.

Cleaning of the diaper area with Liniderm at each diaper change during 28 days
Active Comparator: Wipes
Free-fragrance baby wipes The product will be used on the diaper area by parents/ caregivers at each diaper change.
Cleaning of the diaper area with wipes at each diaper change during 28 days
Active Comparator: Water
Water and cotton pads The product will be used on the diaper area by parents/ caregivers at each diaper change.
Cleaning of the diaper area with water and cotton pads at each diaper change during 28 days

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Number of infants who had at least one episode of diaper rash
Time Frame: 28 days

Every day, in a daily log, parents/ caregivers will report the presence or not of a diaper rash.

At the end of the follow-up, the investigator must identify infant who have had at least one episode of diaper rash.

28 days

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Severity of diaper rash episodes: rating
Time Frame: Continuously for 28 days

Every day, parents/ caregivers will report the rating of erythema if applicable using an illustrated scale ( 4 points scale).

The rating scale is: 0 (Normal skin), 1 (Mild erythema/ pink skin), 2 (Severe erythema/ red skin) and 3 (Erythema with skin erosion).

Continuously for 28 days
Severity of diaper rash episodes: extent
Time Frame: Continuously for 28 days

Every day, parents/ caregivers will report the extent of erythema if applicable using an illustrated scale ( 4 points scale).

The extent scale is: 0 (Healthy skin), 1 (On the folds/ small spread), 2 (On the convexity/ moderate spread) and 3 (Wide spread).

Continuously for 28 days
Safety of the cleaning method
Time Frame: Continuously for 28 days

Every day, parents will report intolerance/ discomfort felt. Also, at each visit, the investigator will carry out a clinical examination of the diaper area; the investigator will assess the tolerance using a 4-points Likert scale.

The 4-points Likert scale is: Bad (0), Moderate (1), Good (2) or Very good (3)

Continuously for 28 days
Skin evaluation on the genital area
Time Frame: 0, 14 and 28 days

Assessment of the skin integrity using a numeric scale (6 points) by the paediatrician at each visit.

The numeric scale is: 0 (No rash), 1 (Mild irritation or rash), 2 (Moderate irritation or rash), 3 (Considerable irritation or rash), 4 (Extreme irritation or rash) and 5 (Extreme erythema involving entire area, oozing papules, pustules erosion).

Skin colour measurements using a Chroma Meter.

0, 14 and 28 days
Paediatrician satisfaction
Time Frame: 14 and 28 days

The paediatrician's satisfaction (regarding performance) will be assessed for each infant using a 4-point Likert scale.

The 4-point Likert scale is: Bad (0), Moderate (1), Good (2) or Very good (3)

14 and 28 days
Well-being
Time Frame: 0, 14 and 28 days
The well-being of infant will be assessed by parents at each visit. Questions will be about crying, agitation, tension and scratching (Yes/ No).
0, 14 and 28 days
Parents satisfaction
Time Frame: 14 and 28 days

The parents' satisfaction (regarding performance and safety) will be assessed using a 4-point Likert scale.

The 4-point Likert scale is: Bad (0), Moderate (1), Good (2) or Very good (3)

14 and 28 days

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Collaborators

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

August 2, 2018

Primary Completion (Actual)

March 18, 2019

Study Completion (Actual)

March 18, 2019

Study Registration Dates

First Submitted

July 16, 2018

First Submitted That Met QC Criteria

August 20, 2018

First Posted (Actual)

August 21, 2018

Study Record Updates

Last Update Posted (Actual)

April 4, 2019

Last Update Submitted That Met QC Criteria

April 2, 2019

Last Verified

April 1, 2019

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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