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Effect of Consuming a Combination of Probiotic Strains and a Combination of Plant Extracts and a Probiotic Strain on the Production and Nutritional Composition of Breast Milk

Multicenter, Randomized, Double-blind Parallel Group Pilot Study to Evaluate the Effect of Consuming a Combination of Probiotic Strains and a Combination of Plant Extracts and a Probiotic Strain on the Production and Nutritional Composition of Breast Milk

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04639232
Enrollment
58
Registered
2020-11-20
Start date
2021-01-30
Completion date
2022-12-31
Last updated
2025-02-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Milk Expression

Keywords

Breastfeeding, Galactogogue, Plant extracts, Probiotics

Brief summary

The objective of this trial is to evaluate the effect of the consumption of a combination of probiotic strains (Prob-milk) and of a combination of plant extracts plus an inactivated probiotic strain (VoluntasProb) on the production volume and the nutritional composition and the microbiota. of breast milk in lactating women.

Detailed description

Previous studies have shown the galactogogue effect of fenugreek, fennel, and milk thistle. However, to date no study has considered the evaluation of all three extracts. Additionally, certain probiotic strains of Lactobacillus and Bifidobacterium also appear to increase milk production in animal studies. The objective of this trial is to evaluate the effect of the consumption of a combination of probiotic strains (Prob-milk) and of a combination of plant extracts plus an inactivated probiotic strain (VoluntasProb) on the production volume and the nutritional composition and the microbiota. of breast milk in lactating women. This is a preliminary study whose purpose is to gather information for future studies.

Interventions

DIETARY_SUPPLEMENTPlacebo

Each participant will consume 6 capsules daily, 2 in every meal, without any restriction in the diet nor in their habits of life.

DIETARY_SUPPLEMENTProb-milk

Each participant will consume 6 capsules daily, 2 in every meal, without any restriction in the diet nor in their habits of life.

DIETARY_SUPPLEMENTVoluntas-Prob

Each participant will consume 6 capsules daily, 2 in every meal, without any restriction in the diet nor in their habits of life.

Sponsors

Biosearch S.A.
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

1. Lactating women between 18 and 45 years old, who have given birth to a healthy baby at term (born between 37 and 42 weeks). 2. Who have the perception of having little volume of milk or a nutritional composition of milk that is not adequate for their baby 3. That they are between week 2 and week 6 of breastfeeding, and that at the time of beginning the study they are not supplementing with formula milk the feeding of their baby. 4. That they have the firm intention of breastfeeding for 28 more days. 5. Women who agree to participate and have read, understood and signed the informed consent

Exclusion criteria

1. Suffering from any disease that may hinder or prevent breastfeeding 2. Being currently consuming or having consumed in the two weeks prior to the study a probiotic or a supplement with plant extracts. 3. Being consuming any drug that can alter the volume or composition of breast milk. 4. Have an allergy to any antibiotics or peanuts 5. Have an allergy to any of the components of the products under study

Design outcomes

Primary

MeasureTime frameDescription
Microbiota of breast milk28 daysLoad of Lactobacillus, Bifidobacterium, Staphylococcus, Streptococcus in breast milk
Volume of breast milk28 daysThe volume of breast milk production will be measured as the difference in weight in grams of the child before and after the first and last feeding of the day, measured on two consecutive days. It should be collected on the first two days before starting treatment and two days in a row separated by one week during treatment.

Secondary

MeasureTime frameDescription
Measurement of IgA in breast milk28 daysAnalysis of the concentration of IgA (ug/mL) in breast milk
Baby feces microbiota28 daysPresence of Lactobacillus spp, Bifidobacterium spp., Streptococcus spp. Staphylococcus spp, Bacteroides spp, E. coli spp, Clostridium spp in baby faeces
Baby's anthropometric measures_weight28 daysWeight (kg) of the baby at baseline, 14 days and 28 days.
Baby's anthropometric measures_height28 daysHeight (cm) of the baby at baseline, 14 days and 28 days.
Baby's anthropometric measures_BMI28 daysBMI (kg/m2) of the baby at baseline, 14 days and 28 days.
Nutritional composition of breast milk28 daysAnalysis of the content of proteins, fatty acids profile and total fat content, and iron and calcium content in breast milk
Data about the intestinal health of the baby_color of the faeces28 daysData about color of the feces (yellow, mustard, brown, grey, or green)
Data about the intestinal health of the baby_consistency of the feces28 daysData about consistency of the feces (hard lumps, sausage with cracks, soft sausage, mushy (like porridge),or watery)
Data about sleep parameters of the baby28 daysHours of night sleeping per day and hours of total sleeping during the day
Infantile colick symptoms28 daysPresence of infantile colick defined as vigorous and inconsolable crying for more than 3 hours a day for at least 3 weeks
Data about the intestinal health of the baby_stool frequency28 daysData about stool frequency (times per day)
Measurement of IL-8 in breast milk28 daysAnalysis of the concentration of IL-8 (pg/mL) in breast milk

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026