A Study of a Baby Wash/Shampoo and Baby Lotion Versus Baby Wash/Shampoo Alone for Impact on Skin Barrier and Microbiome on Newborns
NCT ID: NCT05589038
Last Updated: 2023-10-10
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
NA
53 participants
INTERVENTIONAL
2022-10-25
2023-06-28
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
OTHER
SINGLE
Study Groups
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Baby Wash/Shampoo
Parent participant will bathe the baby participants using baby wash/shampoo at least 3 times per week, but no more than once daily, up to 4 weeks.
Baby Wash/Shampoo
Parent participant will bathe the baby participant with the baby wash/shampoo at least 3 times per week, but no more than once daily.
Baby Wash/Shampoo + Baby Lotion
Parent participant will bathe the baby participants using baby wash/shampoo at least 3 times per week, but no more than once daily, and apply lotion at least once daily after bathing, for 4 weeks.
Baby Wash/Shampoo
Parent participant will bathe the baby participant with the baby wash/shampoo at least 3 times per week, but no more than once daily.
Baby Lotion
Parent participant will use the baby lotion on baby participants at least once daily.
Interventions
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Baby Wash/Shampoo
Parent participant will bathe the baby participant with the baby wash/shampoo at least 3 times per week, but no more than once daily.
Baby Lotion
Parent participant will use the baby lotion on baby participants at least once daily.
Eligibility Criteria
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Inclusion Criteria
* Baby medically determined to be in overall good health and eligible for study participation. Parent determined to be in generally good health and able to participate fully in the study
For Baby only:
* Healthy, full-term, newborns 0 - 28 days old at start of study, (both vaginal and Caesarean mode of delivery may be included, 37+ weeks gestation)
* Fitzpatrick Skin Types I - VI
For Parent only:
* 18 years of age or older
* Biological, legal guardian and primary caregiver of the baby participant (must be able to present proof of guardianship \[that is, birth certificate along with valid identification {ID} of parent, hospital records, insurance card, et cetera {etc.}\])
* Able to read, write, speak, and understand english
* Has signed the informed consent document (ICD) including Health Insurance Portability and Accountability Act (HIPAA) disclosure
* Has to have access to internet to be able to complete questionnaires and diaries
* Intends to successfully complete the study and is willing and able to follow the participant responsibilities
Exclusion Criteria
* Has known allergies or adverse reactions to common topical skincare products or ingredients in the investigational study materials
* Has self-reported Type 1 or Type 2 diabetes or is taking insulin or another anti-diabetic medication
* Is taking medications that would mask an adverse event (AE) or influence the study results, including: immunosuppressive and steroidal drugs within 3 months before Visit 1 and during the study; non-steroidal anti-inflammatory drugs within 5 days before Visit 1 and during the study; antihistamines within 2 weeks before Visit 1 and during the study; systemic or topical over-the-counter (OTC) or prescription medications that, in the principle investigator (PI)'s judgement, will affect skin condition or interfere with study evaluation (example, antibiotics). Use of acetaminophen as needed is acceptable if it was instructed by the baby's pediatrician. Child vitamins are allowed
* Has a history of or a concurrent health condition/situation which, in the opinion of the PI, may put the individual at significant risk, confound the study results, or interfere significantly with the individual's participation in the study
* Is simultaneously participating in any other type of study or has participated in a study within the past 14 days
* Is an employee/contractor or immediate family member of the PI, study site or sponsor
For Baby only:
* Presents with a skin condition that may influence the outcome of the study (example, psoriasis, eczema, atopic dermatitis, cutaneous xerosis, erythema, or active skin cancer)
* Either biological parent or a sibling has clinically determined atopic dermatitis or asthma
* Clinical grade greater than 0 for rash/irritation or greater or equal to 1 for any of the other clinically assessed parameters
For Parent only:
* Is self-reported to be pregnant or planning to become pregnant during the study
0 Days
28 Days
ALL
Yes
Sponsors
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Johnson & Johnson Consumer Inc. (J&JCI)
INDUSTRY
Responsible Party
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Principal Investigators
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Johnson & Johnson Consumer Inc. (J&JCI) Clinical Trial
Role: STUDY_DIRECTOR
Johnson & Johnson Consumer Inc. (J&JCI)
Locations
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KGL Skin Study Center, LLC
Newtown Square, Pennsylvania, United States
Countries
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References
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Walters RM, Mao G, Gunn ET, Hornby S. Cleansing formulations that respect skin barrier integrity. Dermatol Res Pract. 2012;2012:495917. doi: 10.1155/2012/495917. Epub 2012 Aug 13.
Telofski LS, Morello AP 3rd, Mack Correa MC, Stamatas GN. The infant skin barrier: can we preserve, protect, and enhance the barrier? Dermatol Res Pract. 2012;2012:198789. doi: 10.1155/2012/198789. Epub 2012 Sep 4.
Capone KA, Friscia DL, Nikolovski J, Telofski LS, Stamatas GN. A randomized clinical study on the effects of emollient use on the developing infant skin microbiome and metabolome. Exp Dermatol. 2023 Jan;32(1):75-77. doi: 10.1111/exd.14684. Epub 2022 Oct 20. No abstract available.
Avi Sadeh, D. Sc., Jodi A. Mindell, Ph.D., and Liat Tikotzky, Ph.D. Brief Infant Sleep Questionnaire - Revised Long Form, version January 2020
Other Identifiers
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CCSSKB005013
Identifier Type: OTHER
Identifier Source: secondary_id
CCSSKB005013
Identifier Type: -
Identifier Source: org_study_id
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