Study Results
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View full resultsBasic Information
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TERMINATED
NA
134 participants
INTERVENTIONAL
2008-01-31
2011-03-31
Brief Summary
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Detailed Description
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Prospective studies of the effect of vitamin D supplementation on disease outcomes have not been undertaken in children with IBD to date. We aim to perform a) a randomized controlled trial to compare the efficacy of 3 regimens in treating vitamin D insufficiency in pediatric patients with IBD over a period of 6 weeks. We will also evaluate the effects of each regimen on markers of bone resorption, bone formation and parathyroid hormone levels, and the relationship between the magnitude of gastrointestinal protein loss, as reflected by clearance of fecal alpha -1-antitrypsin, and the efficacy of the treatment. b) We also aim to perform a randomized controlled trial to compare the efficacy of 2 regimens of different doses of oral vitamin D2 in maintaining optimal vitamin D stores in pediatric patients with IBD over a period of 2 years. We intend to study the effect of each regimen on a) bone mass acquisition (measured via DXA and pQCT) and bone strength (measured via pQCT), b) bone formation and resorption markers and parathyroid hormone, and c) disease outcomes and disease severity over the same period of time.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Treatment A
2,000 IU/day of ergocalciferol orally for 6 weeks (control arm)
ergocalciferol
8000 units/ml
Treatment B
2,000 IU/day of cholecalciferol orally for 6 weeks
Cholecalciferol
400 units per drop
Treatment C
50,000 IU of ergocalciferol once a week orally for 6 weeks
ergocalciferol
8000 units/ml
Maintenance A
400 IU/day of ergocalciferol orally over 2 years (control arm)
ergocalciferol
8000 units/ml
Maintenance B
2,000 IU/day of ergocalciferol orally from November 1 to April 30, and 1,000 IU/day of ergocalciferol orally for the remainder of the year over 2 years
ergocalciferol
8000 units/ml
Interventions
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ergocalciferol
8000 units/ml
Cholecalciferol
400 units per drop
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* serum 25OHD level ≤ 20 ng/mL (Treatment Trial)
* serum 25OHD level \> 20 ng/mL (Maintenance Trial)
Exclusion Criteria
* patients on growth hormone, anabolic steroid hormones, calcitonin, bisphosphonates (Maintenance Trial only)
5 Years
21 Years
ALL
No
Sponsors
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National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
NIH
Crohn's and Colitis Foundation
OTHER
NASPGHAN Foundation
OTHER_GOV
Boston Children's Hospital
OTHER
Responsible Party
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Helen Pappa
Assistant Professor
Principal Investigators
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Helen Pappa, MD, MPH
Role: PRINCIPAL_INVESTIGATOR
Boston Children's Hospital
Locations
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Children's Hospital, Boston
Boston, Massachusetts, United States
Countries
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References
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Pappa HM, Mitchell PD, Jiang H, Kassiff S, Filip-Dhima R, DiFabio D, Quinn N, Lawton RC, Bronzwaer ME, Koenen M, Gordon CM. Maintenance of optimal vitamin D status in children and adolescents with inflammatory bowel disease: a randomized clinical trial comparing two regimens. J Clin Endocrinol Metab. 2014 Sep;99(9):3408-17. doi: 10.1210/jc.2013-4218. Epub 2014 Jun 13.
Pappa HM, Mitchell PD, Jiang H, Kassiff S, Filip-Dhima R, DiFabio D, Quinn N, Lawton RC, Varvaris M, Van Straaten S, Gordon CM. Treatment of vitamin D insufficiency in children and adolescents with inflammatory bowel disease: a randomized clinical trial comparing three regimens. J Clin Endocrinol Metab. 2012 Jun;97(6):2134-42. doi: 10.1210/jc.2011-3182. Epub 2012 Mar 28.
Other Identifiers
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