Effect of Probiotics Consumed During Pregnancy on the Incidence of Mastitis

Sponsor
Biosearch S.A. (Industry)
Overall Status
Recruiting
CT.gov ID
NCT04032899
Collaborator
(none)
480
3
2
26.5
160
6

Study Details

Study Description

Brief Summary

The aim of the present study is to evaluate the effect of consumption during pregnancy and the lactation period of the probiotic L. fermentum CECT5716 on the incidence of mastitis.

Bacterial load and immunological parameters in breast milk, parameters related to breastfeeding as well as health parameters of the mother and baby will also be evaluated.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: Lactobacillus fermentum CECT5716
  • Dietary Supplement: Maltodextrin
N/A

Detailed Description

Pregnancy and lactation are important moments for the child that will determine their development and future health. One of the key processes is when the microbiota is established in the baby. Contamination during delivery with the mother's vaginal flora, as well as bacteria from the microbiota of breast milk, are important sources for intestinal colonization. However, the mother's microbiota can suffer alterations that affect the health of the mother and can also have an effect on the baby.

Mastitis is a condition of the mammary gland that can affect between 3-30% of women during the period of lactation and is the first cause of abandonment of it. It is associated with a dysbiosis with the proliferation of microorganisms in milk such as Staphylococcus and Streptococcus.

Previous studies carried out with the strain L. fermentum CECT5716 have demonstrated a powerful regulating activity of the microbiota of breast milk that translates into a preventive and curative effect on mastitis. The highest incidence of mastitis occurs during the first weeks after delivery, so the investigator's working hypothesis is that the modulation of the maternal microbiota before delivery would improve the effectiveness of the probiotic strain consumption.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
480 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Prevention
Official Title:
Multicenter, Randomized, Double-blind, Controlled Parallel Nutritional Intervention Study to Evaluate the Effect of Consumption During Pregnancy and the Lactation Period of Lactobacillus Fermentum CECT5716 on the Incidence of Mastitis
Actual Study Start Date :
Apr 15, 2019
Anticipated Primary Completion Date :
Jun 30, 2021
Anticipated Study Completion Date :
Jun 30, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: L. fermentum CECT5716 3x109 ufc

Volunteers will take 1 capsule per day with L. fermentum CECT5716 3x109 cfu mixed with maltodextrin from week 28-32 of gestation up to 16 weeks after delivery.

Dietary Supplement: Lactobacillus fermentum CECT5716
Each participant will consume 1 capsule per day in one of the main meals without any restriction in the diet or in their life habits.

Placebo Comparator: Maltodextrin

Volunteers will take 1 capsule per day with maltodextrin from week 28-32 of gestation up to 16 weeks after delivery.

Dietary Supplement: Maltodextrin
Each participant will consume 1 capsule per day in one of the main meals without any restriction in the diet or in their life habits.

Outcome Measures

Primary Outcome Measures

  1. Incidence of mastitis [4 months]

    Total events during breastfeeding period /total number of participants

Secondary Outcome Measures

  1. Microbiota of breast milk [4 months]

    Load of Staphylococcus, S. aureus, S. epidermidis, Streptococcus, Lactobacillus and L. fermentum CECT5716 in breast milk

Other Outcome Measures

  1. Recurrence of mastitis [4 months]

    Reappearance of mastitis symptoms

  2. Breast pain questionnaire [4 months]

    Mcgill Pain Questionnaire, validated for Spain. The Questionnaire has four dimensions or scales of measures of intensity: Sensory Intensity Value, Affective Intensity Value, Current Intensity Value, and Evaluative Intensity Value. The scales of the Questionnaire were calculated as the sum of their items. Those items were re-corded as 1 if the participant described the pain or as 0 if the participant did not report that type of pain. Thus, the sensory intensity scale can range from 0 to 33, as the full scale is formed by 33 items. The Affective scale varies from 0 to 19, and the scales of Current Intensity and Evaluative Intensity can range from 0 to 6 and 5, respectively

  3. Time of Breastfeeding [4 months]

    Date of initiation and cessation of breastfeeding

  4. Percentage of infants breastfeed [4 months]

    Percentage of infants who receive exclusive breastfeeding

  5. Measurement of biomarkers of inflammation in breast milk [4 months]

    Concentration of IL-1b, IL-6, IL-8, IL-17, TNF-α in breast milk

  6. Immunoglobulins in breast milk [4 months]

    Concentration of IgA, IgG1, IgG2, IgG3, IgG4 and IgM in breast milk

  7. Minerals in breast milk [4 months]

    Concentration of calcium (μg/L), magnesium (μg/L) and potassium (μg/L) in breast milk

  8. Baby feces microbiota [4 months]

    Presence of Escherichia coli, Clostridium, Bacteroides, Bifidobacteria, Lactobacillus and L. fermentum CECT5716 in baby feces

  9. Data on childbirth [4 months]

    Incidence of cesareans and incidence of antibiotic use during delivery.

  10. Baby's anthropometric measures [16 weeks]

    Anthropometric measures of the baby (weight in kg, height in cm and BMI in kg/m2) at birth, 4 weeks, 8 weeks and 16 weeks.

  11. Data about the intestinal health of the baby [4 months]

    Data about stool frequency, colour and consistency of the feces and gasses

  12. Data about sleep parameters of the baby [4 months]

    Hours of night sleeping per day and hours of total sleeping during the day

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 45 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Normal development of pregnancy

  • Single fetus pregnancy

  • Be in week 28-32 of pregnancy

  • Intention to breastfeed the child for 16 weeks

Exclusion Criteria:
  • Having a breast disease that hinders or prevents breastfeeding

  • Have been taking probiotic supplements 2 weeks before starting the study

  • Have a low expectation of adherence to the study protocol

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hospital Costa del Sol Marbella Andalucia Spain 29603
2 Hospital Campus de la Salud Granada Grabada Spain 18007
3 Hospital Virgen de las Nieves Granada Spain 18014

Sponsors and Collaborators

  • Biosearch S.A.

Investigators

  • Principal Investigator: Nicolás Mendoza, MD, PhD, Professor of Gynecology at the Faculty of Medicine of the University of Granada

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Biosearch S.A.
ClinicalTrials.gov Identifier:
NCT04032899
Other Study ID Numbers:
  • P045
First Posted:
Jul 25, 2019
Last Update Posted:
Oct 19, 2020
Last Verified:
Oct 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Biosearch S.A.
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 19, 2020