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Recruiting NCT07508917

Effects of 5-Methyltetrahydrofolic Acid Supplementation on Maternal Health and One-Carbon Metabolism During Lactation

Conditions: Breastfeeding

Sex: Female
Ages: 18 Years – 42 Years
Healthy volunteers: No
Phase: PHASE1, PHASE2
Enrollment: 36
Sponsor: Fundació Sant Joan de Déu

Location: Hospital Sant Joan de Deu Barcelona Barcelona

Summary

This double-blind, randomized, placebo-controlled parallel trial evaluates the effects of maternal 5-methyltetrahydrofolate (5-MTHF) supplementation during breastfeeding. Thirty-six lactating mother-infant dyads will be randomized (1:1) to receive 5-MTHF or placebo for 6 weeks, stratified by infant sex and mode of delivery. Tolerability and adverse events will be monitored. Pre- and post-intervention assessments include breast milk one-carbon metabolites and oligosaccharides; maternal plasma one-carbon metabolites and metabolic health markers. Maternal mental health will be evaluated using the SCL-90-R questionnaire. A follow-up visit at 4 months will reassess infant anthropometry and microbiome outcomes.

Eligibility Criteria

Inclusion Criteria: * Maternal age between 18 and 42 years * Gestational age at birth ≥ 37 weeks. * Exclusive breastfeeding at enrollment. * Infant age 0-1 months Exclusion Criteria: * Multiple pregnancy * Presence of disease or malformations in the infant. * Weight-Standard Deviation Score \< -1 at enrollment. * Use of folate-containing multivitamin supplements during breastfeeding

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07508917). StuddyBuddy aggregates publicly available trial information.