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Daily Use of Lipikar Balm AP From Birth in Infants at High Risk of Developing Atopic Dermatitis

Primary Purpose

Atopic Dermatitis, Eczema, Asthma

Status
Terminated
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Lipikar Balm AP
Sponsored by
Cosmetique Active International
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Atopic Dermatitis focused on measuring Dermatitis, Eczema, Skin diseases, Skin barrier, Prevention, Infant, Moisturizer, Emollient, Asthma, Food allergy, Allergic rhinitis

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Women 18 years of age or older at the time of consent
  • At least 16 weeks pregnant
  • Women with a high risk of having a child with atopic dermatitis defined as having one parent or related sibling of the child to be born who currently (or previously) suffers from atopic dermatitis and who also suffers from asthma or allergic rhinitis
  • Be willing to use the body cleanser Lipikar Syndet and to apply Lipikar Balm AP (if randomized to group 1) every day from birth for 2 years
  • Capable of giving informed consent and the consent must be obtained prior to any study related procedures

Exclusion Criteria:

  • Preterm birth defined as birth before 37 weeks of gestation
  • Major congenital anomaly at birth
  • Presence of significant dermatitis at birth
  • Any medical problem at birth that would prevent the daily use of Lipikar Syndet and/or Lipikar Balm AP (regardless of the group the subject was randomized to) or would prevent evaluation of the skin for the presence of atopic dermatitis

Sites / Locations

  • Hamzavi Dermatology/Dermatology Specialists of Canton
  • Hamzavi Dermatology
  • Lynderm Research
  • Windsor Clinical Research

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

No Intervention

Arm Label

Group 1: Lipikar Balm AP

Group 2: No intervention control group

Arm Description

Daily application of Lipikar Balm AP starting at birth

Subjects may use a moisturizer if they wish to but no instruction or product is provided

Outcomes

Primary Outcome Measures

Proportion of Infants Who Develop Atopic Dermatitis
Proportion of infants who develop atopic dermatitis at two years for infants randomized to Lipikar Balm AP as compared to infants randomized to the no intervention control group

Secondary Outcome Measures

Proportion of Infants Who Develop Asthma
Proportion of infants who develop asthma at two years for infants randomized to Lipikar Balm AP as compared to infants randomized to the no intervention control group
Proportion of Infants Who Develop a Food Allergy
Proportion of infants who develop a food allergy at two years for infants randomized to Lipikar Balm AP as compared to infants randomized to the no intervention control group
Influence of the Presence of Mutation in the Filaggrin Gene on the Proportion of Infants Who Develop Atopic Dermatitis
Influence of the presence of mutation in the filaggrin gene on the proportion of infants who develop atopic dermatitis at two years for infants randomized to Lipikar Balm AP as compared to infants randomized to the no intervention control group
Influence of the Presence of Mutation in the Filaggrin Gene on the Proportion of Infants Who Develop Asthma
Influence of the presence of mutation in the filaggrin gene on the proportion of infants who develop asthma at two years for infants randomized to Lipikar Balm AP as compared to infants randomized to the no intervention control group
Influence of the Presence of Mutation in the Filaggrin Gene on the Proportion of Infants Who Develop a Food Allergy
Influence of the presence of mutation in the filaggrin gene on the proportion of infants who develop a food allergy at two years for infants randomized to Lipikar Balm AP as compared to infants randomized to the no intervention control group
Time of Onset of Asthma in Infants
Time of onset of asthma in infants randomized to Lipikar Balm AP as compared to infants randomized to the no intervention control group
Time of Onset of Food Allergy in Infants
Time of onset of food allergy in infants randomized to Lipikar Balm AP as compared to infants randomized to the no intervention control group
Adverse Events (AEs) Collection
Adverse events (Skin AEs, asthma, food allergies, allergic rhinitis and any AE related to Lipikar Syndet, Lipikar Balm AP (group 1) or any other moisturizer application (group 2) will be collected.
Time of Onset of Atopic Dermatitis
Time of onset of atopic dermatitis in infants randomized to Lipikar Balm AP as compared to infants randomized to the no intervention control group

Full Information

First Posted
April 10, 2012
Last Updated
March 23, 2016
Sponsor
Cosmetique Active International
Collaborators
Innovaderm Research Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT01577628
Brief Title
Daily Use of Lipikar Balm AP From Birth in Infants at High Risk of Developing Atopic Dermatitis
Official Title
Randomized, Multicentric, Controlled Study on the Daily Use of Lipikar Balm AP From Birth in Infants at High Risk of Developing Atopic Dermatitis
Study Type
Interventional

2. Study Status

Record Verification Date
March 2016
Overall Recruitment Status
Terminated
Why Stopped
Sponsor Decision
Study Start Date
June 2012 (undefined)
Primary Completion Date
February 2013 (Actual)
Study Completion Date
February 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Cosmetique Active International
Collaborators
Innovaderm Research Inc.

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
There is a lack of prospective scientific data on the regular use of moisturizers in patients at risk of developing atopic dermatitis. Although generally accepted and widely used for secondary prevention, emollients have not been studied as a primary prevention strategy. Strategies previously studied for the prevention of atopic dermatitis include maternal and child's dietary manipulations, allergens avoidance, delay of food introduction, exclusive breastfeeding and probiotic supplementation. Despite years of research, none of those strategies yielded to strong evidence of a protective effect. There is therefore a need to explore novel strategies. There is a need to compare the cumulative incidence rate of atopic dermatitis in newborns using a standard bathing and moisturizing routine with a good moisturizer to a non interventional group. This 2-year study will recruit approximately four hundred and sixty (460) pregnant women with a first degree relative of the child to be born who currently has (or previously had) a diagnosis of atopic dermatitis in order to study approximately 200 eligible newborns in each of the two study groups at the beginning of the study. Pregnant women will be randomized (1:1) to either daily use of the moisturizer Lipikar Balm AP (applied to their infant) starting from birth (Group 1) immediately after bathing or to no intervention (Group 2).
Detailed Description
To be eligible, pregnant women must be at least 16 weeks pregnant. Expecting mothers (or the father of the infant to be born) or related sibling of the child to be born must meet or previously have met criteria for atopic dermatitis. In addition, one of the parents or sibling of the child to be born must suffer from allergic rhinitis or asthma. Pregnant women will be randomized at screening and their infant will be seen at 1 month, 6 months, 12 months (1 year) and 24 months (2 years) after birth. Women randomized to group 1 will be requested to use the same body cleanser (Lipikar Syndet) and to apply Lipikar Balm AP to their child once daily immediately after bathing on a well blotted skin (within 3 minutes of bathing) to the entire body (including the face) from birth, while women randomized to group 2 will be in a non-interventional control group. The presence of atopic dermatitis (using Hanifin's criteria(1)) and study products use will be assessed at 1 month, 6 months, 12 months and 24 months after birth. A buccal smear will be sampled from all infants at 1 month after birth for the genotyping of filaggrin (FLG) gene. In addition, adverse events evaluation and parent questioning on infants development of food allergies and asthma will be performed at 1 month, 3 months (telephone visit), 6 months, 12 months and 24 months after birth. Infants will be followed for a total of two years after birth. Lipikar Balm AP is a commonly used cosmetic moisturizer commercially available in many countries including Canada. This moisturizer is recommended for extreme dryness and atopy-prone skin in babies, children and adults. It contains shea butter, paraffin, waxes and vegetable oils. The high content in shea butter and the fraction chosen showed a greater expression of constitutive ceramids forming the barrier function of the skin (data on file at La Roche-Posay).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atopic Dermatitis, Eczema, Asthma, Food Allergies, Allergic Rhinitis
Keywords
Dermatitis, Eczema, Skin diseases, Skin barrier, Prevention, Infant, Moisturizer, Emollient, Asthma, Food allergy, Allergic rhinitis

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
2 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Group 1: Lipikar Balm AP
Arm Type
Other
Arm Description
Daily application of Lipikar Balm AP starting at birth
Arm Title
Group 2: No intervention control group
Arm Type
No Intervention
Arm Description
Subjects may use a moisturizer if they wish to but no instruction or product is provided
Intervention Type
Drug
Intervention Name(s)
Lipikar Balm AP
Intervention Description
Daily application of Lipikar Balm AP starting at birth
Primary Outcome Measure Information:
Title
Proportion of Infants Who Develop Atopic Dermatitis
Description
Proportion of infants who develop atopic dermatitis at two years for infants randomized to Lipikar Balm AP as compared to infants randomized to the no intervention control group
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Proportion of Infants Who Develop Asthma
Description
Proportion of infants who develop asthma at two years for infants randomized to Lipikar Balm AP as compared to infants randomized to the no intervention control group
Time Frame
2 years
Title
Proportion of Infants Who Develop a Food Allergy
Description
Proportion of infants who develop a food allergy at two years for infants randomized to Lipikar Balm AP as compared to infants randomized to the no intervention control group
Time Frame
2 years
Title
Influence of the Presence of Mutation in the Filaggrin Gene on the Proportion of Infants Who Develop Atopic Dermatitis
Description
Influence of the presence of mutation in the filaggrin gene on the proportion of infants who develop atopic dermatitis at two years for infants randomized to Lipikar Balm AP as compared to infants randomized to the no intervention control group
Time Frame
2 years
Title
Influence of the Presence of Mutation in the Filaggrin Gene on the Proportion of Infants Who Develop Asthma
Description
Influence of the presence of mutation in the filaggrin gene on the proportion of infants who develop asthma at two years for infants randomized to Lipikar Balm AP as compared to infants randomized to the no intervention control group
Time Frame
2 years
Title
Influence of the Presence of Mutation in the Filaggrin Gene on the Proportion of Infants Who Develop a Food Allergy
Description
Influence of the presence of mutation in the filaggrin gene on the proportion of infants who develop a food allergy at two years for infants randomized to Lipikar Balm AP as compared to infants randomized to the no intervention control group
Time Frame
2 years
Title
Time of Onset of Asthma in Infants
Description
Time of onset of asthma in infants randomized to Lipikar Balm AP as compared to infants randomized to the no intervention control group
Time Frame
2 years
Title
Time of Onset of Food Allergy in Infants
Description
Time of onset of food allergy in infants randomized to Lipikar Balm AP as compared to infants randomized to the no intervention control group
Time Frame
2 years
Title
Adverse Events (AEs) Collection
Description
Adverse events (Skin AEs, asthma, food allergies, allergic rhinitis and any AE related to Lipikar Syndet, Lipikar Balm AP (group 1) or any other moisturizer application (group 2) will be collected.
Time Frame
2 years
Title
Time of Onset of Atopic Dermatitis
Description
Time of onset of atopic dermatitis in infants randomized to Lipikar Balm AP as compared to infants randomized to the no intervention control group
Time Frame
2 years

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Women 18 years of age or older at the time of consent At least 16 weeks pregnant Women with a high risk of having a child with atopic dermatitis defined as having one parent or related sibling of the child to be born who currently (or previously) suffers from atopic dermatitis and who also suffers from asthma or allergic rhinitis Be willing to use the body cleanser Lipikar Syndet and to apply Lipikar Balm AP (if randomized to group 1) every day from birth for 2 years Capable of giving informed consent and the consent must be obtained prior to any study related procedures Exclusion Criteria: Preterm birth defined as birth before 37 weeks of gestation Major congenital anomaly at birth Presence of significant dermatitis at birth Any medical problem at birth that would prevent the daily use of Lipikar Syndet and/or Lipikar Balm AP (regardless of the group the subject was randomized to) or would prevent evaluation of the skin for the presence of atopic dermatitis
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Robert Bissonnette, MD, FRCPC
Organizational Affiliation
Innovaderm Research
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hamzavi Dermatology/Dermatology Specialists of Canton
City
Canton
State/Province
Michigan
ZIP/Postal Code
48187
Country
United States
Facility Name
Hamzavi Dermatology
City
Fort Gratiot
State/Province
Michigan
ZIP/Postal Code
48059
Country
United States
Facility Name
Lynderm Research
City
Markham
State/Province
Ontario
ZIP/Postal Code
L3P 1A8
Country
Canada
Facility Name
Windsor Clinical Research
City
Windsor
State/Province
Ontario
ZIP/Postal Code
N8W 5L7
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No

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Daily Use of Lipikar Balm AP From Birth in Infants at High Risk of Developing Atopic Dermatitis

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