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NOT YET RECRUITING
NCT07444008
NA

Randomized, Blinded, Placebo-Controlled Evaluation of BioAmicus Complete

Sponsor: NovoNatum Ltd

View on ClinicalTrials.gov

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

DIETARY_SUPPLEMENT

BioAmicus Complete

BioAmicus Complete (oral drops; a mixture of 10 strains of lacto- and bifidobacteria)

DIETARY_SUPPLEMENT

Placebo

Sunflower oil

Locations (1)

City outpatient # 43

Saint Petersburg, Russia