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Fish Oil Supplementation to Pregnant Women in China

Fish Oil Supplementation to Prevent Preterm Delivery in China: A Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02770456
Acronym
FOPCHIN
Enrollment
5531
Registered
2016-05-12
Start date
2008-03-31
Completion date
2016-04-30
Last updated
2016-05-12

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

Conditions

Premature Birth

Keywords

fish oil, preterm birth, pregnancy, China, prevention

Brief summary

This randomized controlled trial with fish oil supplementation to pregnant women conducted in areas of China, which are generally low in fish intake and low income, aims at answering the following primary questions: * Is a dose of 2.0 g/d long chain n-3 fatty acids efficient in preventing preterm birth * Is a dose of 0.5 g/d long chain n-3 fatty acids efficient in preventing preterm birth * Is a dose of 0.5 g/d as efficient as a dose of 2.0 g/d in affecting timing of spontaneous delivery in the preterm period

Detailed description

The basic design is that of a randomized controlled trial with three groups randomized in ratios of 1:1:1. Two different doses of long chain n-3 fatty acids are tested against zero grams long chain n-3 fatty acids (lc-n3FA). These are provided in similarly looking gelatine capsules with either fish oil, a mixture (1:3) of fish oil and olive oil, or olive oil. Eligible women are randomized at around gestation weeks 16-24 and are asked to take the capsules until they have completed the preterm period (i.e. at 37 full gestation weeks) or until they deliver. Women are asked to complete questionnaires at randomization about diet and other baseline information, and again in gestation week 30 and after delivery. The trial is undertaken at hospitals in the two provinces of Gan-Su and Shaanxi. The three randomization groups will be compared with respect to proportions of preterm delivery. Cox regression will be used to compare the groups with respect to rates of spontaneous deliveries while accounting for elective delivery by regarding these as censoring events.

Interventions

DIETARY_SUPPLEMENTHigh dose fish oil

Four 0.72-gram gelatine capsules per day with fish oil providing 2.0 g/d lc-n3FA

DIETARY_SUPPLEMENTLow dose fish oil

Four 0.72-gram gelatine capsules per day with a mixture of fish oil and olive oil providing 0.5 g/d lc-n3FA

DIETARY_SUPPLEMENTOlive oil

Four 0.72-gram gelatine capsules per day with olive oil providing 0 g/d lc-n3FA

Sponsors

Shanghai Institute of Planned Parenthood Research
CollaboratorOTHER_GOV
Centre for Fetal Programming, Denmark
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
20 Years to 44 Years
Healthy volunteers
Yes

Inclusion criteria

* Pregnancy without known complications

Exclusion criteria

* Regular user of fish oil * Regular user of NSAIDs * Known twin pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Premature birth20 weeks on average, from randomization at gestation weeks 16-24 until on average gestation week 40Delivery occurring earlier than 259 gestation days

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 1, 2026