Efficacy of Vitamin D Supplementation for Children With Bronchiolitis

Sponsor
Sohag University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05795933
Collaborator
(none)
146
1
2
13
11.2

Study Details

Study Description

Brief Summary

Vitamin D plays an important role in enhancing mucosal immune defense, decreasing excessive inflammation, and increasing mucociliary clearance. Experimental studies have shown that vitamin D reduces inflammation of epithelial cells in airways infected with Respiratory Syncytial Virus and confers antiviral effects. Furthermore, several studies have shown lower serum vitamin D levels in hospitalized children with bronchiolitis. However, studies on the efficacy of Vitamin D supplementation for children with bronchiolitis are scarce with inconsistent findings. In this study, we aim to evaluate the efficacy of vitamin D supplementation in children with bronchiolitis.

Condition or Disease Intervention/Treatment Phase
  • Drug: Vitamin D3
Phase 2/Phase 3

Detailed Description

Bronchiolitis is the most frequent lower respiratory tract infection in children under two years of age, which represents a major cause of medical visits, hospital admissions, and death. This disease predominantly affects small airways with acute inflammatory edema epithelial cells, excess mucus production, and bronchospasm. The most commonly involved organisms are Respiratory Syncytial Virus (accounting for 60% of cases), followed by Rhinovirus, Parainfluenza, Metapneumovirus, Influenza, and Adenovirus. Certain factors are associated with a higher risk of severe bronchiolitis, such as prematurity, chronic lung disease, cardiac disease, immunodeficiency, neuromuscular disease, and Down syndrome.

Diagnosis of bronchiolitis relies on a constellation of clinical manifestations, including respiratory distress and wheezing preceded by viral upper respiratory tract prodrome in children under two years of age. Common manifestations of bronchiolitis are rhinorrhea, cough, wheezing, tachypnea, and increased work of breathing, including nasal flaring, retractions, and grunting. Management of bronchiolitis is mainly supportive, aiming at maintaining adequate oxygenation and hydration.

Given the high burden of bronchiolitis and the lack of specific treatment, studies have investigated several therapeutic options. One of these potential therapies is vitamin D. Vitamin D is a fat-soluble vitamin that is mainly formed in the skin after exposure to ultraviolet rays, while less than 10% is obtained from dietary sources. Besides regulation of calcium and phosphorus homeostasis, vitamin D plays an important role in enhancing mucosal immune defense, decreasing excessive inflammation, and increasing mucociliary clearance. Vitamin D deficiency is common among children, particularly in developing countries, and has been linked to an increased risk of several diseases, including bronchiolitis, pneumonia, and otitis media.

Experimental studies have shown that vitamin D reduces inflammation of epithelial cells in airways infected with Respiratory Syncytial Virus and confers antiviral effects. Furthermore, several studies have shown lower serum vitamin D levels in hospitalized children with bronchiolitis. However, studies on the efficacy of Vitamin D supplementation for children with bronchiolitis are scarce with inconsistent findings.

In this study, we aim to evaluate the efficacy of vitamin D supplementation in children with bronchiolitis.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
146 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Two groups of children with bronchiolitis: Study group: will receive a single dose of intramuscular 200,000 IU vitamin D3 within 24 hours of admission. Control group: will receive the standard recommended dose of vitamin D3 as 400 IU/day orallyTwo groups of children with bronchiolitis:Study group: will receive a single dose of intramuscular 200,000 IU vitamin D3 within 24 hours of admission. Control group: will receive the standard recommended dose of vitamin D3 as 400 IU/day orally
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Efficacy of Vitamin D Supplementation for Children With Bronchiolitis at Sohag University Hospital
Actual Study Start Date :
Apr 1, 2023
Anticipated Primary Completion Date :
Apr 1, 2024
Anticipated Study Completion Date :
May 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Study group

Children receive a single dose of intramuscular 200,000 IU vitamin D3

Drug: Vitamin D3
A single dose of intramuscular 200,000 IU vitamin D3 within 24 hours of admission
Other Names:
  • Cholecalciferol
  • Devarol
  • No Intervention: Control group

    Children receiving only the standard recommended dose of vitamin D3 as 400 IU/day orally

    Outcome Measures

    Primary Outcome Measures

    1. Time from randomization to discharge [4 weeks]

      Time from randomization to hospital discharge (in hours)

    Secondary Outcome Measures

    1. Time from randomization to discontinuation of oxygen therapy [4 weeks]

      Time from randomization to discontinuation of oxygen therapy (in hours)

    2. Time from randomization to discontinuation of intravenous fluids [4 weeks]

      Time from randomization to discontinuation of intravenous fluids (in hours)

    3. Time from randomization to meeting discharge criteria [4 weeks]

      Time from randomization to meeting hospital discharge criteria (in hours)

    4. Time from hospital admission to discharge [4 weeks]

      Time from hospital admission to discharge (in hours)

    5. Blood level of 25-hydroxycholecalciferol [On day 3 after randomization]

      Blood level of 25-hydroxycholecalciferol

    6. Serum level of ionized calcium [On day 3 after randomization]

      Serum level of ionized calcium

    7. Admission to pediatric intensive care unit [4 weeks]

      Proportion of patients admitted to pediatric intensive care unit

    8. Intubation [4 weeks]

      Proportion of patients who underwent endotracheal intubation

    9. Mortality [4 weeks]

      Proportion of patients who died during hospital admission

    10. Bronchodilator therapy [4 weeks]

      Proportion of patients who received bronchodilator therapy

    11. Systemic steroids [4 weeks]

      Proportion of patients who received systemic steroids

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    3 Months to 24 Months
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Age between 3 to 24 months.

    • Clinical diagnosis of first episode of bronchiolitis

    • First 24 hours of admission.

    • Stable or decreasing requirement for oxygen on 2 measurements 2 hours apart.

    • Pulse rate less than 180 beat/minute.

    • Respiratory rate less than 80 breath/min.

    • Oxygen supplementation < 40% Fraction of inspired oxygen or < 2 L/min by nasal prong

    • Not on high flow nasal cannula, continuous positive airway pressure, or mechanical ventilation at the time of enrollment.

    Exclusion Criteria:

    .• History of previous episodes of wheezing.

    • History of apnea

    • Need for positive pressure support or high flow nasal cannula at the time of enrollment.

    • Chronic lung disease (requiring home oxygen, or pulmonary hypertension)

    • Cardiac disease (cyanotic, hemodynamically significant [requiring diuretics], or pulmonary hypertension).

    • Neuromuscular disease.

    • Metabolic disease.

    • Immunodeficiency.

    • Chromosomal abnormalities.

    • Craniofacial malformation

    • Hemoglobinopathy.

    • Hypercalcemia

    • Chromosomal abnormalities

    • Use of large doses of vitamin D (> 400 IU/day) in the last month.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Sohag University Hospital Sohag Egypt 82524

    Sponsors and Collaborators

    • Sohag University

    Investigators

    • Study Chair: Mostafa A Mohammed, MD, PhD, Sohag University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Youstina Safwat Labib, Pediatric Resident, Sohag University
    ClinicalTrials.gov Identifier:
    NCT05795933
    Other Study ID Numbers:
    • Soh-Med-23-03-11MS
    First Posted:
    Apr 3, 2023
    Last Update Posted:
    Apr 4, 2023
    Last Verified:
    Apr 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Youstina Safwat Labib, Pediatric Resident, Sohag University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 4, 2023