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Completed

NCT Number: NCT01601847

Wheezing in Black Preterm Infants: Impact of Vitamin D Supplementation Strategy

The goal of this study is to identify a vitamin D supplementation strategy that best promotes the lung, immune, and overall health of black infants born preterm (28-36 weeks gestational age). This is a high risk population that seems to have unique vitamin D needs, and inappropriate supplementation may promote wheezing or allergy. The results of this study will help form nutritional recommendations for the approximately 100,000 black infants born at 30-36 weeks gestational age in the U.S. every year.

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Key information

Age range

Up to 1 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Montefiore Medical Center, New York, United States

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About this study

Black infants face the highest rates of prematurity in the U.S. (18%), have high rates of prematurity-associated wheezing illnesses, and tend to have lower vitamin D levels. The goal of this [comparative effectiveness] study is to identify a vit. D supplementation strategy that minimizes recurrent wheezing in infancy. Long recognized as important for bone health, a growing body of evidence suggests that vit. D may play a role in the regulation and development of many organ systems. The D pathway regulates lung inflammation and impacts morphogenesis, structure, and cell growth and survival in bronchial smooth muscle. Vit. D exposure has the potential to skew cytokine expression from a Th1 (less allergic) to a Th2 (more allergic) phenotype. Due to their developmental immaturity, preterm infants may be particularly vulnerable to any positive or negative effects of vit. D supplementation on the lung, airway, and immune system. Our preliminary data, supported by the literature, suggests that overly aggressive vit. D supplementation may inadvertently increase wheezing in infancy in black, but not white, preterm infants; however, vit. D deficiency could theoretically also increase wheezing via vulnerability to respiratory pathogens. The proposed study is a randomized clinical trial comparing the effect of two different enteral vitamin D supplementation strategies on recurrent wheezing in infancy in 300 black infants born preterm at 28 0/7-36 6/7 wks gestational age, a population for whom neither vit. D requirements nor optimal vit. D serum levels have been established. The investigators will test two strategies: (I) sustained supplementation until 6 mo. of age adjusted for prematurity, and (II) cessation of supplementation when a minimum dietary intake of 200 IU/day is reached. The specific aims are to characterize the effect of each strategy on (aim 1) recurrent wheezing and (aim 2) allergic sensitization and atopy. The investigators will (aim 3) explore the relationship between vit. D serum levels and recurrent wheezing. The investigators hypothesize that strategy II will be more effective in promoting pulmonary health by minimizing recurrent wheezing, allergic sensitization, and overall healthcare utilization, and will be sufficient to prevent clinical vit. D deficiency. The investigators also hypothesize that optimal vit. D serum levels will be lower than the norms for other populations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 28 0/7-36 6/7 weeks gestational age (GA) at birth;
  • family identifies the child as black or African American;
  • < 28 days of supplemental oxygen (subsequent oxygen therapy for < 72 hrs for a brief subsequent illness or surgery will be allowed);
  • admitted to a participating site NICU, special care nursery, transitional care nursery, or well-baby nursery as a neonate; and
  • < 40 weeks corrected GA at enrollment.

Exclusion criteria

  • BPD (> 28 days of supplemental oxygen);
  • pre-existing diagnosis of moderate to severe osteopenia of prematurity and/or alkaline phosphatase > 700;
  • history of fracture;
  • gastrointestinal surgery, including for NEC;
  • known gastrointestinal malabsorption;
  • major congenital anomaly;
  • congenital pulmonary or airway disorder (e.g., cystic fibrosis, tracheomalacia, swallowing disorder, bronchopulmonary sequestration);
  • documented wheezing or stridor prior to enrollment;
  • previous vit. D supplementation with > 400 IU/day;
  • family plans to move more than 60 miles from CWRU or other pre-defined radius at other sites;
  • baseline hypo- or hypercalcemia, hypo- or hyperphosphatemia; and
  • baseline 25(OH) D level < 10 ng/ml.

Treatment and study plan

Cholecalciferol

Dietary Supplement

Once the dietary intake of vitamin D has exceeded 200 IU/Day, the infants will receive placebo until they are 6 months of age adjusted for prematurity

Cholecalciferol

Drug

Infants will receive cholecalciferol 400 IU/day PO until they are 6 months of age adjusted for prematurity

Other names: D-Vi-Sol, Vitamin D

Primary outcomes

  1. Number of Infants With Recurrent Wheezing

    Time frame: up to 12 months adjusted age

    Recurrent wheezing was defined as more than 1 episode of wheezing reported during the study period. Separate episodes were defined as occurring at least 2 weeks apart.

Secondary outcomes

  1. Number With Infants With Allergic Sensitization as Measured by the PhadiaTop Infant Assay

    Time frame: Measured at the 12 month adjusted age visit

    Measured using the Phadiatop Infant IgE panel

  2. Bone Density

    Time frame: Measured at the 12 month adjusted age visit

    Measured by bone speed of sound (ultrasound)

Sponsors and collaborators

Lead sponsor

Case Western Reserve University

Other

Collaborators

  • National Heart, Lung, and Blood Institute (NHLBI)
  • Office of Dietary Supplements (ODS)

Registry information

Acronym: D-Wheeze

Important dates

Study start
2013
Primary completion
2017
Study completion
2017
First posted
May 18, 2012
Registry last updated
Jun 8, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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