The effect of fish-oil supplementation on pregnancy outcomes in mother and infant

Not Applicable

• Conditions: Condition 1: Pregnancy, childbirth and the puerperium. Condition 2: Pregnancy, childbirth and the puerperium. Condition 3: Pregnancy, childbirth and the puerperium. Condition 4: Pregnancy, childbirth and the puerperium. Condition 5: Pregnancy, childbirth and the puerperium. Condition 6: Pregnancy, childbirth and the puerperium. Condition 7: Certain conditions originating in the perinatal period. Condition 8: Certain conditions originating in the perinatal period.; Gestational [pregnancy-induced] hypertension with significant proteinuria; Diabetes mellitus in pregnancy, unspecified; Preterm labour and delivery; Single delivery by caesarean section; Mental disorders and diseases of the nervous system complicating pregnancy, childbirth and the puerperium; Pregnancy-related condition, unspecified; Fetus and newborn affected by maternal nutritional disorders; Disorders related to short gestation and low birth weight, not elsewhere classified

• Registration Number: IRCT2013100914957N1
• Lead Sponsor: ational Public-Health Management Center (NPMC)

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 150

Inclusion Criteria

Healthy pregnant women in 16-20 weeks of pregnancy; Aged 18-35 years; 5th pregnancy or less; Singleton pregnancy; No history of infertility and premature birth; Not having history of depression or postpartum depression; Edinburgh depression score less than 23; Absence of known placenta previa or cerclage in this pregnancy; No adverse event occurred 6 months before the study
Exclusion criteria: Smoking or drugs using ;consumption of more than two servings fish per week; Having bleeding disorders or taking anticoagulants; BMI more than 30; participating in another study; Wanting to change living area in the next 6 months; No access to call phone; Being illiterate or unable to answer questions; History of sensitivity to fish oil or other fish products; sensitivity to gelatin; participation in other intervention study; Not willingness to participate; known underlying disease including heart, kidney, stomach, lung, thyroid or autoimmune diseases, diabetes, impaired glucose tolerance in pregnancy, epilepsy, essential hypertension,hyperlipidemia

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Postpartum Depression. Timepoint: 6-8 weeks after childbirth. Method of measurement: Edinburgh Depression Scale.;Newborn Weight. Timepoint: Childbirth. Method of measurement: By means of newborns scale into gram.;Infant Neurodevelopment. Timepoint: 4 and 6 month. Method of measurement: ASQ Questionnare.