Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06570889

VItamin D in pregnanCy for prevenTion Of eaRlY Childhood Asthma

VItamin D in pregnanCy for prevenTion Of eaRlY Childhood Asthma (VICTORY)

Status
Recruiting
Phase
Phase 3
Study type
Interventional
Enrollment
2,000 (estimated)
Sponsor
Professor Klaus Bønnelykke · Academic / Other
Sex
Female
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

The overall aim of the study is to develop a nutritional preventive vitamin D supplementation strategy in pregnancy for early childhood asthma/persistent wheeze during the first three years of life as we hypothesize that supplementation in higher doses than recommended could reduce the risk of disease development.

Detailed description

Randomization of 2000 pregnant women to vitamin D of high-dose (3200 IU/day) vitamin D vs placebo on top of the recommended 400 IU/day. Supplementation begins in gestational week 24 (22-26) until 1 week after delivery. Allocation to the trial will be determined based on the pre-interventional maternal blood levels of EPA+DHA with a dried blood screening test. Women with high levels (above 4.7% of total fatty acids) will be assigned to the vitamin D RCT. Maternal blood will be used for genetic, metabolomic and proteomic profiling. A 3-year follow-up of the children with longitudinal registration of parent reported symptoms, diagnoses, medication use, and hospitalizations will be performed. The primary outcome is persistent wheeze or asthma until age 3 years, with predefined analyses of effect modification by maternal genotypes. Secondary outcomes are lower respiratory tract infections, gastrointestinal infections, croup, troublesome lung symptoms, eczema, allergy, bone fractures, developmental milestones, mental health, cognition, and growth until age 3 years. A follow-up on both primary and secondary outcomes is planned after unblinding, from age 3 to 6 years.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTCholecalciferol D3Oral intake of 1 capsule per day from week 22-26 in pregnancy to 1 week after delivery
OTHEROlive oilOral intake of 1 capsule per day from week 22-26 in pregnancy to 1 week after delivery

Timeline

Start date
2024-12-20
Primary completion
2026-10-01
Completion
2033-03-01
First posted
2024-08-26
Last updated
2025-09-30

Locations

1 site across 1 country: Denmark

Source: ClinicalTrials.gov record NCT06570889. Inclusion in this directory is not an endorsement.