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The Effect of Omega 3 on Pregnancy Complicated by Asymmetrical Intrauterine Growth Restriction

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02696577
Enrollment
68
Registered
2016-03-02
Start date
2015-03-31
Completion date
2016-02-29
Last updated
2016-03-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intrauterine Growth Restriction

Brief summary

Intrauterine growth restriction is a common and complex obstetric problem. Intrauterine growth restriction is noted to affect approximately 10-15 % of pregnant women. Intrauterine growth restriction is diagnosed antenatal; however, some of these fetuses, especially if unscreened during pregnancy, may be detected only in the neonatal period. It is very important for obstetricians and perinatologists to identify growth restricted fetuses, because this fetal condition is associated with significant perinatal morbidity and mortality. Omega 3 is composed of polyunsaturated fatty acids with a double bond at the third carbon atom from the end of the carbon chain. The fatty acids have two ends, the carboxylic acid end, which is considered the beginning of the chain, thus alpha, and the methyl end, which is considered the tail of the chain, thus omega. Omega3 improve fetal wellbeing by two mechanisms: Firstly, maternal and docosahexaenoic acid supplementation during pregnancy and lactation normalizes intrauterine growth restriction induced changes in adipose deposition and visceral PPARγ expression. Secondly, maternal docosahexaenoic acid supplementation increases serum adiponectin, as well as adipose expression of adiponectin and adiponectin receptors. Novel findings suggest that maternal docosahexaenoic acid supplementation normalize adipose dysfunction and promote adiponectin-induced improvements in metabolic function in intrauterine growth restriction

Interventions

DRUGOmega 3

Sponsors

Assiut University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 35 Years
Healthy volunteers
No

Inclusion criteria

* Age: from 20 - 35 years old. * Pregnant from 30 week to 32 week gestation. * Singleton pregnancy with asymmetrical intrauterine growth restriction . * Normal uterine and umbilical Doppler indices at time of recruitment.

Exclusion criteria

* Multiple gestations. * Hypertensive women. * Premature rupture of membranes. * Abnormal Doppler indices in the form of Doppler blood flow indices \> 2 standard deviation , absent diastolic flow and lastly; reversed flow. * Congenital fetal malformation. * Pregnancy complicated by antepartum hemorrhage. * Marked decrease in Amniotic fluid volume.

Design outcomes

Primary

MeasureTime frame
Estimated fetal weight (gm)1 year

Secondary

MeasureTime frame
The changes in Doppler blood flow indices in both uterine arteries1 year
The changes in Doppler blood flow indices in umbilical artery1 year
Fetal weight at the time of delivery (gm) ,1 year
Number of babies admitted to neonatal intensive care unit.1 year

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 11, 2026