Effect of an Inhibitor of Cholesterol Absorption on Vitamin D Levels
Primary Purpose
Vitamin D Deficiency
Status
Completed
Phase
Phase 4
Locations
Brazil
Study Type
Interventional
Intervention
Ezetimibe
Cholecalciferol
Placebo
Sponsored by
About this trial
This is an interventional basic science trial for Vitamin D Deficiency focused on measuring vitamin D, absorption, ezetimibe
Eligibility Criteria
Inclusion Criteria:
- Medical students of the HCPA
Exclusion Criteria:
- Body mass index >+ 25 or < 18.5 kg/m2
- Known liver, kidney or endocrine disease
- Known malabsorption
- Use of supplements of calcium and/or vitamin Danticonvulsants, barbiturates, or glucocorticoids
- Travel outside the Brazilian south region during the previous 120 days
Sites / Locations
- Hospital de Clínicas de Porto Alegre
Arms of the Study
Arm 1
Arm 2
Arm Type
Placebo Comparator
Active Comparator
Arm Label
Placebo + Cholecalciferol
Ezetimibe + Cholecalciferol
Arm Description
The groups will be randomized to ezetimibe or placebo. All participants will receive orally a cholecalciferol capsule.
The groups will be randomized to ezetimibe or placebo. All participants will receive orally a cholecalciferol capsule.
Outcomes
Primary Outcome Measures
25-hydroxyvitamin D
The groups will be randomized to ezetimibe 10 mg for 5 days or placebo. On the fifth day, they should came after an overnight fast for blood tests collection [25(OH)D, PTH, calcium, albumin]. Next, all participants will receive orally a cholecalciferol 50,000 IU capsule and a snack containing 15g of fat. Participants will return 14 days after that for a second blood test.
Secondary Outcome Measures
Full Information
NCT ID
NCT02234544
First Posted
August 31, 2014
Last Updated
April 7, 2015
Sponsor
Federal University of Rio Grande do Sul
1. Study Identification
Unique Protocol Identification Number
NCT02234544
Brief Title
Effect of an Inhibitor of Cholesterol Absorption on Vitamin D Levels
Official Title
Estudo clínico Randomizado, Controlado e Duplo-cego do Impacto da inibição de um Transportador de Membrana do Colesterol na absorção da Vitamina D
Study Type
Interventional
2. Study Status
Record Verification Date
April 2015
Overall Recruitment Status
Completed
Study Start Date
October 2014 (undefined)
Primary Completion Date
April 2015 (Actual)
Study Completion Date
April 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Federal University of Rio Grande do Sul
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Double-blind randomized controlled trial to evaluate the serum levels of 25(OH)D after a single oral dose of cholecalciferol 50,000 IU plus ezetimibe or placebo.
Differences between the serum levels of 25(OH)D in response to cholecalciferol plus ezetimibe compared to cholecalciferol plus placebo.
Detailed Description
Objectives: To evaluate the serum levels of 25(OH)D after a single oral dose of cholecalciferol 50,000 IU plus ezetimibe or placebo.
Experimental design: Double-blind randomized controlled trial. Research location: Porto Alegre Clinical Hospital (HCPA), RS, Brazil. Participants: Medical residents of the HCPA. Intervention: The groups will be randomized to ezetimibe 10 mg for 5 days or placebo. On the fifth day, they should came after an overnight fast for blood tests collection [25(OH)D, PTH, calcium, albumin]. Next, all participants will receive orally a cholecalciferol 50,000 IU capsule and a snack containing 15g of fat. Participants will return 14 days after that for a second blood test.
Statistical Analysis: Paired samples t-test or Wilcoxon signed rank-test will be used for comparing variables in two distinct moments (before cholecalciferol and 14 days after). The correlation between the numerical variables will be evaluated by the Spearman's correlation coefficient. A p value of less than 0.05 was considered statistically significant.
Expected results: Differences between the serum levels of 25(OH)D in response to cholecalciferol plus ezetimibe compared to cholecalciferol plus placebo.
Cost/benefit of the project: This is a low budget and minimal risks study that will contribute to a better understanding of the absorptive process of vitamin D and the effect of ezetimibe on its absorption.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vitamin D Deficiency
Keywords
vitamin D, absorption, ezetimibe
7. Study Design
Primary Purpose
Basic Science
Study Phase
Phase 4
Interventional Study Model
Factorial Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
52 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Placebo + Cholecalciferol
Arm Type
Placebo Comparator
Arm Description
The groups will be randomized to ezetimibe or placebo. All participants will receive orally a cholecalciferol capsule.
Arm Title
Ezetimibe + Cholecalciferol
Arm Type
Active Comparator
Arm Description
The groups will be randomized to ezetimibe or placebo. All participants will receive orally a cholecalciferol capsule.
Intervention Type
Drug
Intervention Name(s)
Ezetimibe
Intervention Description
The groups will be randomized to ezetimibe 10 mg for 5 days or placebo. On the fifth day, they should came after an overnight fast for blood tests collection [25(OH)D, PTH, calcium, albumin]. Next, all participants will receive orally a cholecalciferol 50,000 IU capsule and a snack containing 15g of fat. Participants will return 14 days after that for a second blood test.
Intervention Type
Drug
Intervention Name(s)
Cholecalciferol
Other Intervention Name(s)
Vitamin D
Intervention Description
All participants will receive orally a cholecalciferol 50,000 IU capsule and a snack containing 15g of fat. Participants will return 14 days after that for a second blood test.
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
The groups will be randomized to ezetimibe 10 mg for 5 days or placebo. On the fifth day, they should came after an overnight fast for blood tests collection [25(OH)D, PTH, calcium, albumin]. Next, all participants will receive orally a cholecalciferol 50,000 IU capsule and a snack containing 15g of fat. Participants will return 14 days after that for a second blood test.
Primary Outcome Measure Information:
Title
25-hydroxyvitamin D
Description
The groups will be randomized to ezetimibe 10 mg for 5 days or placebo. On the fifth day, they should came after an overnight fast for blood tests collection [25(OH)D, PTH, calcium, albumin]. Next, all participants will receive orally a cholecalciferol 50,000 IU capsule and a snack containing 15g of fat. Participants will return 14 days after that for a second blood test.
Time Frame
up to 24 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Medical students of the HCPA
Exclusion Criteria:
Body mass index >+ 25 or < 18.5 kg/m2
Known liver, kidney or endocrine disease
Known malabsorption
Use of supplements of calcium and/or vitamin Danticonvulsants, barbiturates, or glucocorticoids
Travel outside the Brazilian south region during the previous 120 days
Facility Information:
Facility Name
Hospital de Clínicas de Porto Alegre
City
Porto Alegre
State/Province
RS
ZIP/Postal Code
90035-903
Country
Brazil
12. IPD Sharing Statement
Citations:
PubMed Identifier
26208795
Citation
Silva MC, Faulhauber GAM, Leite EN, Goulart KR, Ramirez JMA, Cocolichio FM, Furlanetto TW. Impact of a cholesterol membrane transporter's inhibition on vitamin D absorption: A double-blind randomized placebo-controlled study. Bone. 2015 Dec;81:338-342. doi: 10.1016/j.bone.2015.07.022. Epub 2015 Jul 21.
Results Reference
derived
Learn more about this trial
Effect of an Inhibitor of Cholesterol Absorption on Vitamin D Levels
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