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

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Key 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
20132015

Study locations (1)

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.

Open NCT01838447 on ClinicalTrials.gov

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