- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03229317
Respiratory Outcome of Children From the FEPED Cohort (RESPIFEPED)
January 14, 2026 updated by: Assistance Publique - Hôpitaux de Paris
Respiratory Outcome According to Early Maternal Vitamin D Status During Pregnancy in Children Aged 5 to 6 Years Old
Early lung function deficits represent a significant risk factor for the evolution toward chronic obstructive pulmonary disease later in life.
Prematurity and in utero tobacco smoke exposure are already known to predispose children to develop a non-reversible obstructive ventilatory defect in adulthood.
The role of vitamin D status during pregnancy is less certain.
In humans, low vitamin D concentrations during pregnancy are associated to an increased risk of asthma in children.
In murine models, low vitamin D concentrations during pregnancy are associated to structural abnormalities of the airways in mouse pups.
Investigators hypothesized that vitamin D play a role in early airways development, from the first trimester of pregnancy.
To bring arguments to this hypothesis, the investigators will study the association of airway resistance in children aged 5 to 6 years old with the concentration of vitamin D during the first trimester of pregnancy in their mothers.
Study Overview
Detailed Description
Children aged 5 to 6 years old will be included from the FEPED cohort.
The FEPED cohort is a cohort of French pregnant women designed to study the association between vitamin D status during pregnancy and the risk of pre-eclampsia.
Vitamin D concentration at first and third trimester of pregnancy as well as in cord blood is available for 1400 women.
Investigators will include 200 children born from these women.
Children will undergo lung function tests and prick-tests and parents will answer the ISAAC questionnaire that is a standardised questionnaire designed to evaluate asthma and rhinitis symptoms.
The main outcome of this study will be specific airway resistance.
The investigators will look for an association between specific airway resistance and vitamin D concentration measured during the first trimester of pregnancy in their mothers.
Study Type
Observational
Enrollment (Actual)
142
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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Paris
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Paris, Paris, France, 75019
- Robert Debré Hospital
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Paris, Paris, France, 75012
- Armand Trousseau Hospital
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Paris, Paris, France, 75015
- Necker Enfants-malades Hospital
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
5 years to 6 years (Child)
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
term-born child (gestational age ≥ 37 weeks of post-menstrual age) whose mother was included in the FEPED cohort, with measure of vitamin D concentration available at the first and third trimester of pregnancy and in cord blood
Description
Inclusion Criteria:
- term-born child (gestational age ≥ 37 weeks of post-menstrual age) whose mother was included in the FEPED cohort
- measure of vitamin D concentration available at the first and third trimester of pregnancy and in cord blood
- cord blood sample available for DNA extraction
- child's age between 5 and 6 years old at the time of participation
- written informed consent obtained from the legal guardian of the child
- health insurance
Exclusion Criteria:
- parent's' refusal
- underlying disease that does not allow the performance of lung function tests
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Specific airway resistance measured by plethysmography
Time Frame: 1 day
|
The measure of this outcome will be compared between children with a concentration of vitamin D during the first trimester of pregnancy < 20 ng/ml and children with a concentration ≥ 20 ng/ml
|
1 day
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Interrupter airway resistance measured by the interrupter technique using a pneumotachograph
Time Frame: 1 day
|
This secondary outcome is another way to measure airway resistance.
The measure of this outcome will be also compared between children with a concentration of vitamin D during the first trimester of pregnancy < 20 ng/ml and children with a concentration ≥ 20 ng/ml
|
1 day
|
|
Residual functional capacity measured by the helium dilution technique
Time Frame: 1 day
|
This secondary outcome is another lung function parameter that will allow to evaluate lung volumes of the participants.
The measure of this outcome will also be compared between children with a concentration of vitamin D during the first trimester of pregnancy < 20 ng/ml and children with a concentration ≥ 20 ng/ml
|
1 day
|
|
Occurrence of one wheezing episode
Time Frame: 1 day
|
1 day
|
|
|
Age of the first wheezing episode
Time Frame: 1 day
|
1 day
|
|
|
Occurrence of Asthma at age 3 years old
Time Frame: 1 day
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1 day
|
|
|
Occurrence of Asthma at age 5 or 6 years old
Time Frame: 1 day
|
1 day
|
|
|
Allergenic sensitizations determined by skin prick-tests
Time Frame: 1 day
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1 day
|
|
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Genotype of 4 single nucleotide polymorphisms related to vitamin D metabolism
Time Frame: 1 day
|
1 day
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Principal Investigator: Alice HADCHOUEL, MD, PhD, Assistance Publique - Hôpitaux de Paris
- Study Chair: Alexandra BENACHI, MD, PhD, Assistance Publique - Hôpitaux de Paris
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Chawes BL, Bonnelykke K, Stokholm J, Vissing NH, Bjarnadottir E, Schoos AM, Wolsk HM, Pedersen TM, Vinding RK, Thorsteinsdottir S, Arianto L, Hallas HW, Heickendorff L, Brix S, Rasmussen MA, Bisgaard H. Effect of Vitamin D3 Supplementation During Pregnancy on Risk of Persistent Wheeze in the Offspring: A Randomized Clinical Trial. JAMA. 2016 Jan 26;315(4):353-61. doi: 10.1001/jama.2015.18318.
- Litonjua AA, Carey VJ, Laranjo N, Harshfield BJ, McElrath TF, O'Connor GT, Sandel M, Iverson RE Jr, Lee-Paritz A, Strunk RC, Bacharier LB, Macones GA, Zeiger RS, Schatz M, Hollis BW, Hornsby E, Hawrylowicz C, Wu AC, Weiss ST. Effect of Prenatal Supplementation With Vitamin D on Asthma or Recurrent Wheezing in Offspring by Age 3 Years: The VDAART Randomized Clinical Trial. JAMA. 2016 Jan 26;315(4):362-70. doi: 10.1001/jama.2015.18589.
- Wolsk HM, Harshfield BJ, Laranjo N, Carey VJ, O'Connor G, Sandel M, Strunk RC, Bacharier LB, Zeiger RS, Schatz M, Hollis BW, Weiss ST, Litonjua AA. Vitamin D supplementation in pregnancy, prenatal 25(OH)D levels, race, and subsequent asthma or recurrent wheeze in offspring: Secondary analyses from the Vitamin D Antenatal Asthma Reduction Trial. J Allergy Clin Immunol. 2017 Nov;140(5):1423-1429.e5. doi: 10.1016/j.jaci.2017.01.013. Epub 2017 Mar 9.
- Gazibara T, den Dekker HT, de Jongste JC, McGrath JJ, Eyles DW, Burne TH, Reiss IK, Franco OH, Tiemeier H, Jaddoe VW, Duijts L. Associations of maternal and fetal 25-hydroxyvitamin D levels with childhood lung function and asthma: the Generation R Study. Clin Exp Allergy. 2016 Feb;46(2):337-46. doi: 10.1111/cea.12645.
- Lange P, Celli B, Agusti A, Boje Jensen G, Divo M, Faner R, Guerra S, Marott JL, Martinez FD, Martinez-Camblor P, Meek P, Owen CA, Petersen H, Pinto-Plata V, Schnohr P, Sood A, Soriano JB, Tesfaigzi Y, Vestbo J. Lung-Function Trajectories Leading to Chronic Obstructive Pulmonary Disease. N Engl J Med. 2015 Jul 9;373(2):111-22. doi: 10.1056/NEJMoa1411532.
- Postma DS, Bush A, van den Berge M. Risk factors and early origins of chronic obstructive pulmonary disease. Lancet. 2015 Mar 7;385(9971):899-909. doi: 10.1016/S0140-6736(14)60446-3. Epub 2014 Aug 11.
- Belgrave DC, Buchan I, Bishop C, Lowe L, Simpson A, Custovic A. Trajectories of lung function during childhood. Am J Respir Crit Care Med. 2014 May 1;189(9):1101-9. doi: 10.1164/rccm.201309-1700OC.
- Gonsard A, Marquant F, Elie C, Le Bourgeois M, Houdouin V, Delclaux C, Beydon N, Bellino A, Souberbielle JC, Sermet-Gaudelus I, Delacourt C, Benachi A, Hadchouel A. Specific airway resistance according to early maternal vitamin D status during pregnancy in children aged 5 to 6 years old from the FEPED cohort (RESPIFEPED). Eur J Pediatr. 2025 Feb 5;184(2):176. doi: 10.1007/s00431-024-05954-0.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 31, 2018
Primary Completion (Actual)
December 16, 2020
Study Completion (Actual)
December 16, 2020
Study Registration Dates
First Submitted
July 3, 2017
First Submitted That Met QC Criteria
July 24, 2017
First Posted (Actual)
July 25, 2017
Study Record Updates
Last Update Posted (Actual)
January 15, 2026
Last Update Submitted That Met QC Criteria
January 14, 2026
Last Verified
January 1, 2026
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- K160907J
- 2017-A01193-50 (Other Identifier: IDRCB)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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