Effect Of Lactobacillus GG on Atopic March
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|ClinicalTrials.gov Identifier: NCT01891916|
Recruitment Status : Unknown
Verified July 2013 by Roberto Berni Canani, Federico II University.
Recruitment status was: Recruiting
First Posted : July 3, 2013
Last Update Posted : July 16, 2013
|Condition or disease||Intervention/treatment||Phase|
|Cow's Milk Allergy Atopic Disease||Dietary Supplement: Extensively hydrolyzed casein formula + LGG||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||180 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||None (Open Label)|
|Official Title:||Preventive Effect of Lactobacillus GG on Atopic Manifestation in Children With Cow's Milk Allergy|
|Study Start Date :||October 2008|
|Estimated Primary Completion Date :||December 2014|
|Estimated Study Completion Date :||December 2014|
No Intervention: extensively hydrolysed casein formula
extensively hydrolysed casein formula
Active Comparator: Extensively hydrolyzed casein formula + LGG
Extensively hydrolized formula plus LGG
Dietary Supplement: Extensively hydrolyzed casein formula + LGG
Extensively hydrolyzed formula containing Lactobacillus GG
Other Name: Extensively hydrolyzed formula plus LGG
- Occurrence of allergic manifestations [ Time Frame: 3 yrs ]Occurrence of allergic manifestations in children with CMA including atopic eczema, allergic urticaria, asthma, allergic rhinitis.Information on social and demographic factors, family and living conditions, and smoking habits will be documented. Unscheduled visit will be made when possible allergic symptoms will appear. Every 12 months sensitization to common dietary and respiratory antigens will be assessed by skin prick tests (SPT) and prick by prick tests.
- Allergic sensitization [ Time Frame: 3 yrs ]Every 12 months sensitization to common dietary and respiratory antigens will be assessed by skin prick tests (SPT) and prick by prick tests.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01891916
|Contact: Roberto Berni Canani, Phdfirstname.lastname@example.org|
|University of Naples Federico II||Recruiting|
|Contact: Roberto Berni Canani|
|Principal Investigator: Roberto Berni Canani|