CompletedPhase 2NCT01838447
Prevention of Vitamin D Deficiency Following Pediatric CHD Surgery: a Phase II Dose Evaluation Randomized Controlled Trial Comparing Usual Care With a High Dose Pre-operative Supplementation Regimen Based on the Institute of Medicine Daily Upper Tolerable Intake Level
Studying Disorders of vitamin D metabolism
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Children's Hospital of Eastern Ontario
- Principal Investigator
- James D McNally, M.D., Ph.D.Children's Hospital of Eastern Ontario
- Intervention
- Cholecalciferol(dietary_supplement)
- Enrollment
- 46 enrolled
- Eligibility
- 17 years · All sexes
- Timeline
- 2013 – 2015
Study locations (1)
- Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada
Collaborators
The Ottawa Hospital · McGill University · Children's University Hospital, Ireland · Ottawa Hospital Research Institute
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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