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Active, not recruiting Phase 1

Fish Oil Supplementation During Pregnancy for Prevention of Asthma, Eczema and Allergies in Childhood

NCT00798226 · tracked via the Priya Life Science Denmark tracker
Phase
Phase 1
Started
2008-11-26
Last updated
2026-06-05

Condition(s) studied

AsthmaEczemaAllergy

Investigational drug(s) / intervention(s)

n-3 fatty acidolive oil

n-3 fatty acid: Oral intake of 4 capsules daily from week 24 of gestation to 1 week after delivery

olive oil: Oral intake of 4 capsules (1 g) daily from 24 weeks of gestation to 1 week after delivery

Study summary

The aim of this study is to prevent asthma and allergies in childhood by supplementation with fish oil (n-3 fatty acids) to the mother during pregnancy. Paticipants are mother and children participating in the ABC-(Asthma Begins in Childhood)cohort. Mothers are recruited during pregnancy and receive supplement with n-3 fatty acids or olive oil (placebo) from week 24 of gestation to 1 week after delivery. The child is followed with acute and planned visit at the research unit and diagnosis of disease is done in the research unit according to predefined algorithms.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria (mother): * Pregnant women * Living in Sealand, Denmark * Fluent in Danish Language * Willing to let the newborn child participate in the study Exclusion Criteria (mother): * Participating in other clinical trial

Primary outcome measure(s)

  • Persistent wheeze 0 to 3 years of age — 3 years
    Age at onset of persistent wheeze diagnosed according to predefined algorithm of recurrent troublesome lung symptoms, response to treatment and relapse after withdrawal of treatment

Trial sites (2)

FacilityCityRegionStatus
Copenhagen University Hospital of Copenhagen Gentofte Municipality Gentofte
Næstved Hospital, Pediatric Department Næstved Næstved
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT00798226 on ClinicalTrials.gov ↗ ← All trials in Denmark