Study of Vitamin D for the Prevention of Acute Respiratory Infections in Children
Primary Purpose
Acute Respiratory Tract Infections
Status
Completed
Phase
Phase 2
Locations
Chile
Study Type
Interventional
Intervention
Vitamin D3
Placebo
Sponsored by
About this trial
This is an interventional prevention trial for Acute Respiratory Tract Infections focused on measuring Acute respiratory tract infections, vitamin D, cholecalciferol, children, bronchiolitis, pneumonia, prevention
Eligibility Criteria
Inclusion Criteria:
- Children aged 18 to 36 months attending daycare in Santiago, Coyhaique or Punta Arenas.
Exclusion Criteria:
- History of chronic illness requiring immunosuppression
- History of metabolic bone disease
- Use of vitamin D supplementation greater than 400 IU daily, either by milk formula or vitamin supplements in the last 3 months.
- Use of fish oil supplements in the last 3 months.
- Immunodeficiency
- Planned trip to sunny climate during study period.
Sites / Locations
- Hospital de Punta Arenas
- Pontificia Universidad Católica de Chile
- Hospital Las Higueras
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Experimental
Placebo Comparator
Arm Label
5600 IU Vitamin D3
Oral 11200 IU Vitamin D3 weekly
Placebo
Arm Description
Oral 5600 IU Vitamin D3 in liquid weekly during 6 months
Oral 11200 IU Vitamin D3 in liquid weekly during 6 months
Oral placebo in liquid weekly during 6 months
Outcomes
Primary Outcome Measures
Incidence of acute respiratory tract infections
Secondary Outcome Measures
Adverse events
Hospitalizations due to acute respiratory tract infections
Serum cathelicidin levels
Baseline and after 6 months measurement of serum cathelicidin levels.
serum 25-hydroxyvitamin D levels
Baseline and after 6 months measurement of serum 25-hydroxyvitamin D levels.
Viral etiology of ARTIs
Specific virological etiology of ARTIs will be evaluated by polymerase chain reaction in children with febrile ARTIs and with medical diagnosis of bronchiolitis or pneumonia.
Bone metabolism parameters
Baseline and after 6 months measurement of serum parathormone (PTH), alkaline phosphatases, calcium, phosphorus, and urinary calcium/creatinine ratio.
Full Information
NCT ID
NCT02046577
First Posted
January 23, 2014
Last Updated
October 10, 2016
Sponsor
Pontificia Universidad Catolica de Chile
Collaborators
National Fund for Research and Development in Health, Chile, Laboratorio Pasteur
1. Study Identification
Unique Protocol Identification Number
NCT02046577
Brief Title
Study of Vitamin D for the Prevention of Acute Respiratory Infections in Children
Official Title
A Randomized, Double-blind, Controlled Trial of Vitamin D for the Prevention of Acute Respiratory Infections in Children Aged 18 to 36 Months in Santiago, Coyhaique and Punta Arenas, Chile
Study Type
Interventional
2. Study Status
Record Verification Date
October 2016
Overall Recruitment Status
Completed
Study Start Date
February 2014 (undefined)
Primary Completion Date
December 2015 (Actual)
Study Completion Date
May 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Pontificia Universidad Catolica de Chile
Collaborators
National Fund for Research and Development in Health, Chile, Laboratorio Pasteur
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The main purpose of this study is to determine whether weekly oral vitamin D supplementation is effective to prevent acute respiratory tract infections in children. The hypothesis of the study is that vitamin D supplementation reduces the incidence and severity of acute respiratory tract infections in children.
Detailed Description
Acute respiratory tract infections (ARTIs) are associated with high levels of morbidity and socioeconomic impact, particularly affecting young children. Observational studies have shown an association between vitamin D (VD) deficiency and higher incidence and severity of respiratory infections. Chile has a high prevalence of VD deficiency, particularly in the southern regions of the country. The objective of this study is to evaluate the safety and efficacy of oral VD supplementation to decrease the incidence of ARTIs in 275 preschool children. A randomized, placebo-controlled, double-blind study will be performed in Santiago, Coyhaique and Punta Arenas. Children aged 18 to 36 months will be given weekly oral 5600 IU of vitamin D3 (VD3), 11200 IU of VD3, or placebo doses during 6 months.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Respiratory Tract Infections
Keywords
Acute respiratory tract infections, vitamin D, cholecalciferol, children, bronchiolitis, pneumonia, prevention
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
276 (Actual)
8. Arms, Groups, and Interventions
Arm Title
5600 IU Vitamin D3
Arm Type
Experimental
Arm Description
Oral 5600 IU Vitamin D3 in liquid weekly during 6 months
Arm Title
Oral 11200 IU Vitamin D3 weekly
Arm Type
Experimental
Arm Description
Oral 11200 IU Vitamin D3 in liquid weekly during 6 months
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Oral placebo in liquid weekly during 6 months
Intervention Type
Dietary Supplement
Intervention Name(s)
Vitamin D3
Other Intervention Name(s)
Cholecalciferol
Intervention Description
Cholecalciferol administration
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
Placebo liquid
Primary Outcome Measure Information:
Title
Incidence of acute respiratory tract infections
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Adverse events
Time Frame
6 months
Title
Hospitalizations due to acute respiratory tract infections
Time Frame
6 months
Title
Serum cathelicidin levels
Description
Baseline and after 6 months measurement of serum cathelicidin levels.
Time Frame
6 months
Title
serum 25-hydroxyvitamin D levels
Description
Baseline and after 6 months measurement of serum 25-hydroxyvitamin D levels.
Time Frame
6 months
Title
Viral etiology of ARTIs
Description
Specific virological etiology of ARTIs will be evaluated by polymerase chain reaction in children with febrile ARTIs and with medical diagnosis of bronchiolitis or pneumonia.
Time Frame
6 months
Title
Bone metabolism parameters
Description
Baseline and after 6 months measurement of serum parathormone (PTH), alkaline phosphatases, calcium, phosphorus, and urinary calcium/creatinine ratio.
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Months
Maximum Age & Unit of Time
36 Months
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Children aged 18 to 36 months attending daycare in Santiago, Coyhaique or Punta Arenas.
Exclusion Criteria:
History of chronic illness requiring immunosuppression
History of metabolic bone disease
Use of vitamin D supplementation greater than 400 IU daily, either by milk formula or vitamin supplements in the last 3 months.
Use of fish oil supplements in the last 3 months.
Immunodeficiency
Planned trip to sunny climate during study period.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
María L Reyes, M.D.
Organizational Affiliation
Pontificia Universidad Catolica de Chile
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Cecilia Vizcaya, M.D.
Organizational Affiliation
Pontificia Universidad Catolica de Chile
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Arturo Borzutzky, M.D.
Organizational Affiliation
Pontificia Universidad Catolica de Chile
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Catalina Le Roy, M.D.
Organizational Affiliation
Pontificia Universidad Catolica de Chile
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Carlos A. Camargo Jr., M.D. Dr.PH.
Organizational Affiliation
Massachusetts General Hospital, Harvard University
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Karin Brikmann, M.D.
Organizational Affiliation
Hospital Regional de Punta Arenas
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Flavia Chamorro, M.D.
Organizational Affiliation
Hospital de Coyhaique
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Marco Reyes, M.D.
Organizational Affiliation
Hospital de Coyhaique
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Carolina Loureiro, M.D.
Organizational Affiliation
Pontificia Universidad Catolica de Chile
Official's Role
Study Director
Facility Information:
Facility Name
Hospital de Punta Arenas
City
Punta Arenas
State/Province
Magallanes
Country
Chile
Facility Name
Pontificia Universidad Católica de Chile
City
Santiago
State/Province
Región Metropolitana
Country
Chile
Facility Name
Hospital Las Higueras
City
Talcahuano
State/Province
VIII Región
Country
Chile
12. IPD Sharing Statement
Plan to Share IPD
Undecided
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Study of Vitamin D for the Prevention of Acute Respiratory Infections in Children
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