Pregnancy Pregnancy and Childbirth
Conditions
Interventions
Participants are randomly allocated to one of two groups:
1. Intervention group: Participants take capsules containing 360 mg EPA (eicosapentanoic) and 240 mg DHA (docosahexanoic acid)
Sponsors
University of Mostar, School of Medicine
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: 1. Healthy pregnant women 2. Single pregnancy 2. BMI ( < 25kg/m2) 3. Provision of informed consent
Exclusion criteria
Exclusion criteria: 1. Pregnancy terminated as preterm delivery 2. Pregnant women with chronic illness 3. Pregnant women with gestational diabetes mellitus or preeclampsia
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Concentration of n-3 fatty acids in total serum lipids, measured using gas chromatography at the end of pregnancy/delivery 2. Concentration of n-3 fatty acids in umbilical vein serum, measured using gas chromatography at time of birth 3. Concentration of monounsaturated fatty acids in serum total lipids of umbilical vein serum, measured by gas chromatography at time of birth 4. Concentration of monounsaturated fatty acids in serum total lipids of the mother's serum, measured by gas chromatography at the end of pregnancy | — |
Secondary
| Measure | Time frame |
|---|---|
| Weight of mother, measured by weighing scale at recruitment, 20th week of gestation, 30th week of gestation and before delivery | — |
Countries
Bosnia and Herzegovina
Outcome results
None listed