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Randomized, Blinded, Placebo-Controlled Evaluation of BioAmicus Complete
Sponsor: NovoNatum Ltd
Summary
This is a randomized, single-blind, placebo-controlled study to evaluate the efficacy of the dietary supplement BioAmicus Complete (oral drops; a mixture of 10 strains of lacto- and bifidobacteria) in managing functional gastrointestinal disorders and cutaneous symptoms of food allergy in infants during the first months of life. The aim of the study is to assess clinical effects of BioAmicus Complete drops on the symptoms of infantile colic, constipation, diarrhea, gastroesophageal reflux, atopic dermatitis/eczema in full-term newborns during the first months of life. A prospective study comparing two treatment groups: Group 1 (treatment group) - 70 infants. Group 2 (control group) - 70 infants, placebo. The study drug will be taken in 1 time per day within 25 days. Allowed symptomatic therapy includes defoamers (simethicone-based preparations), carminative preparations (dill water (fenhel)), etc.
Official title: A Randomized, Single-Blind, Placebo-Controlled Study to Evaluate the Efficacy of the Dietary Supplement BioAmicus Complete (Oral Drops; a Mixture of 10 Strains of Lacto- and Bifidobacteria) in Managing Functional Gastrointestinal Disorders and Cutaneous Symptoms of Food Allergy in Infants During the First Months of Life
Key Details
Gender
All
Age Range
1 Month - 5 Months
Study Type
INTERVENTIONAL
Enrollment
140
Start Date
2026-02-26
Completion Date
2026-06-30
Last Updated
2026-03-03
Healthy Volunteers
No
Interventions
BioAmicus Complete
BioAmicus Complete (oral drops; a mixture of 10 strains of lacto- and bifidobacteria)
Placebo
Sunflower oil
Locations (1)
City outpatient # 43
Saint Petersburg, Russia