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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COMPLETED
NA
160 participants
INTERVENTIONAL
2016-11-30
2020-12-31
Brief Summary
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Detailed Description
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The study will be divided in 2 parts: The main study (Interventional period) lasts up to the child´s age of one year (52 weeks of life) and the follow-up period up to the second birthday.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
SINGLE
Study Groups
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Intervention: standardized skin care regimen
Intervention: The milk lotion will be applied once daily on the total body including the face by the parents or care givers at home. If bathing is needed, the bathing addendum is used in addition to water.
standardized skin care regimen
Application of a standardized daily skin care regimen:
* milk lotion once daily and
* application of addendum for bathing as needed
Control
In the control group no predetermined or standardized skin care regimen is prescribed.
No interventions assigned to this group
Interventions
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standardized skin care regimen
Application of a standardized daily skin care regimen:
* milk lotion once daily and
* application of addendum for bathing as needed
Eligibility Criteria
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Inclusion Criteria
2. Healthy term newborns (gestational age: completed 37 weeks) born by mothers aged 18-45 years
3. Birth weight between 2.500 - 4.500 g
4. Age at enrolment 14 days
5. Infants at enhanced risk for developing AD (at least one parent or sibling with physician-diagnosed AD, asthma or allergic rhinitis/rhino conjunctivitis as reported by at least by one parent but in otherwise good overall health
6. Infant Nutrition: breastfeeding or cow's-milk based infant formula (including Hypoallergenic (HA) - based formula) feeding or combination
7. Phototype I, II, III or IV according to the Fitzpatrick classification.
Exclusion Criteria
2. Hydrops fetalis
3. Preterm children (\< completed 37th week of gestation)
4. Weight at birth \< 2500 g or \> 4500 g
5. Significant dermatitis at birth except seborrheic dermatitis on the scalp ("cradle cap")
6. Dermatological conditions influencing the study parameters, besides benign transient neonatal diseases
7. Any immunodeficiency disorder
8. Any severe genetic skin disorder
9. Any other serious condition that would make the use of skin care products inadvisable
10. Any other major medical problems that the investigator deems may increase the risk of adverse events with the intervention or in whom assessing the outcomes may be masked by the underlying problem or practically very difficult to assess
11. Participation in another clinical study
12. Reason to presume that the parents are unable to meet the study plan requirements
13. Nutrition: other than breastfeeding or cow's-milk based infant formula (e.g. soybased, goat-milk based formula etc.)
14. History of allergy or intolerance to investigational product's ingredient(s) of at least one subject's parent
15. Current topical or systemic drug treatment
16. Maternal antibiotic therapy in breastfed newborns
17. Infants of mothers supplementing probiotics during pregnancy and/or breastfeeding on a regular basis
14 Days
ALL
Yes
Sponsors
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Charite University, Berlin, Germany
OTHER
HiPP GmbH & Co. Vertrieb KG
INDUSTRY
Responsible Party
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Principal Investigators
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Ulrike Blume-Peytavi, Prof. Dr.
Role: PRINCIPAL_INVESTIGATOR
Charite Universitätsmedizin Berlin
Locations
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Charite Universitätsmedizin Berlin
Berlin, , Germany
Countries
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References
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Simpson EL, Keck LE, Chalmers JR, Williams HC. How should an incident case of atopic dermatitis be defined? A systematic review of primary prevention studies. J Allergy Clin Immunol. 2012 Jul;130(1):137-44. doi: 10.1016/j.jaci.2012.01.075. Epub 2012 Mar 15.
Other Identifiers
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508276
Identifier Type: -
Identifier Source: org_study_id
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