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