Can Supplementation With Lactobacillus Reuteri and Omega-3 Fatty Acids During Pregnancy and Lactation Reduce the Risk of Allergic Disease in Infancy?
NCT ID: NCT01542970
Last Updated: 2012-03-05
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
NA
496 participants
INTERVENTIONAL
2012-02-29
2017-06-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
This is a double blind randomized study. Families with at least one parent/sibling with clinical symptoms/history of allergic disease will be invited to participate in this study. Pregnant mothers will be included in the study at the 20th week of gestation. They will be randomized to 4 study groups, one will receive placebo capsules, the second will receive omega-3 PUFA supplementation and placebo regarding L. reuteri, the third will receive L. reuteri and placebo regarding omega-3 PUFA and the fourth group will receive both omega-3 PUFA and L. reuteri supplementation. Omega-3 supplementation will be given to mothers from pregnancy and lactation while L. reuteri will be given to the mothers during pregnancy and later to the children during the first year of life.The children will be clinically followed by an allergy nurse regularly. Questionnaires regarding data on environment, siblings, pets, breast feeding, smoking exposure, upper respiratory and other infections and clinical symptoms of allergic disease will be filled regularly. Skin prick tests (SPTs) will be performed in the children at 6 and 12 months with milk, egg, wheat, peanut and cat. At 24 months, timothy and birch allergen extracts will be added. A pediatrician will assess the children at 24 months of life and whenever it is needed during the study period. Dietary habits will be assessed during pregnancy (25th gestational week) and 6 months after child birth. Blood samples in the children will be taken from cord blood and at 6, 12 and 24 months of life. Maternal blood samples will be taken at 20th weeks of gestation and at child birth. Milk samples will be collected 1-4 days after partus and monthly during the first 4 months of lactation. Maternal gastrointestinal function will be addressed by validated diary cards. Saliva from the children and fecal samples from mother and child will also be collected according to the following protocol.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Salmon in Pregnancy Study
NCT00801502
Effect of a Mix of Dairy Lipids and Plant Oils in Infant Formula on Omega-3 Fatty Acid in Red Blood Cells
NCT01611649
Effect Of Lactobacillus GG on Atopic March
NCT01891916
Oral Supplement for Pregnant and Lactating Mothers
NCT01073033
Epigenetic Effects in Children With Cow's Milk Allergy Treated With Different Formulas
NCT04184700
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
PREVENTION
QUADRUPLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Placebo
Placebo for both L. reuteri and omega-3 fatty acids.
Placebo
Olive oil
Refined coconut and peanut oil without L. reuteri
2x20 drops daily to the mother from gw 20 and from birth to the child during the first year of life
L. reuteri and placebo
Active Lactobacillus reuteri and placebo for omega-3 fatty acids
Placebo
Olive oil
L. reuteri
The L. reuteri supplementation comprises of L. reuteri suspension 109 colony forming units (CFU) in oil (refined coconut and peanut oil) (20 droplets x 2 daily) to the mothers during pregnancy and 108 CFU (5 droplets x 1) to the children during the first years of life
Omega-3 fatty acids and placebo
Placebo for L. reuteri and active for omega-3 fatty acids
Omega-3 fatty acids
Omega-3 PUFA treatment comprises of maternal supplementation of 3 capsules of Pikasol® (1g capsules containing 640 mg ω-3 PUFA) 2 times daily during pregnancy and lactation.
Refined coconut and peanut oil without L. reuteri
2x20 drops daily to the mother from gw 20 and from birth to the child during the first year of life
L. reuteri and omega-3 fatty acids
Active L. reuteri and active omega-3 fatty acids
L. reuteri
The L. reuteri supplementation comprises of L. reuteri suspension 109 colony forming units (CFU) in oil (refined coconut and peanut oil) (20 droplets x 2 daily) to the mothers during pregnancy and 108 CFU (5 droplets x 1) to the children during the first years of life
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Placebo
Olive oil
Omega-3 fatty acids
Omega-3 PUFA treatment comprises of maternal supplementation of 3 capsules of Pikasol® (1g capsules containing 640 mg ω-3 PUFA) 2 times daily during pregnancy and lactation.
Refined coconut and peanut oil without L. reuteri
2x20 drops daily to the mother from gw 20 and from birth to the child during the first year of life
L. reuteri
The L. reuteri supplementation comprises of L. reuteri suspension 109 colony forming units (CFU) in oil (refined coconut and peanut oil) (20 droplets x 2 daily) to the mothers during pregnancy and 108 CFU (5 droplets x 1) to the children during the first years of life
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* breastfeeding for at least 3 months is mandatory for inclusion in the statistical assessment in the study
Exclusion Criteria
* twin pregnancy
* mothers previously/currently using omega-3 PUFA or probiotic dietary supplementation
* children born before gestational week 33 or seriously ill will be excluded from the study.
18 Years
45 Years
FEMALE
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Ostergotland County Council, Sweden
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Karel Duchén, MD
MD
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Karel M Duchén, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
Ostergotland County Council, Sweden
Maria C Jenmalm, PhD
Role: PRINCIPAL_INVESTIGATOR
Linkoeping University
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Allergicentrum, Universitetssjukhuset
Linköping, , Sweden
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
References
Explore related publications, articles, or registry entries linked to this study.
Al-Kaabawi A, Landberg E, Marti M, Severin E, Tingo L, Duchen K, Jenmalm MC. Effects of maternal allergy and supplementation with omega-3 fatty acid and probiotic on human milk oligosaccharides. Pediatr Allergy Immunol. 2025 Aug;36(8):e70162. doi: 10.1111/pai.70162.
Ahlberg E, Marti M, Govindaraj D, Severin E, Duchen K, Jenmalm MC, Tingo L. Immune-related microRNAs in breast milk and their relation to regulatory T cells in breastfed children. Pediatr Allergy Immunol. 2023 Apr;34(4):e13952. doi: 10.1111/pai.13952.
Huoman J, Martinez-Enguita D, Olsson E, Ernerudh J, Nilsson L, Duchen K, Gustafsson M, Jenmalm MC. Combined prenatal Lactobacillus reuteri and omega-3 supplementation synergistically modulates DNA methylation in neonatal T helper cells. Clin Epigenetics. 2021 Jun 30;13(1):135. doi: 10.1186/s13148-021-01115-4.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
FaLr-013
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.