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Characterization of Hyperparathyroidism and Vitamin D Deficiency in Obesity

Primary Purpose

Vitamin D Deficiency, Secondary Hyperparathyroidism, Obesity

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Ergocalciferol
Cholecalciferol
Sponsored by
Weill Medical College of Cornell University
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Vitamin D Deficiency focused on measuring Vitamin D deficiency, Secondary hyperparathyroidism, Obesity

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Obese subjects with body mass indices greater than 40 kg/m2 or 35 kg/m2 with other medical conditions secondary to obesity Willingness to take vitamin D supplements If baseline vitamin D level is >25 ng/ml subjects will be eligible for the control group If baseline vitamin D level is <25 ng/ml subjects will be eligible for one of the two vitamin D replacement groups Exclusion Criteria: Hypercalcemia Kidney disease Liver disease Malabsorption Prior diagnosis of bone disease Medical conditions requiring daily use of calcium, antacids, or medications known to affect bone metabolism or interact with vitamin D Hypersensitivity to any formulation of vitamin D

Sites / Locations

  • Weill Cornell Medical College

Outcomes

Primary Outcome Measures

Vitamin D (25OHD):RIA and HPLC
Parathyroid hormone (PTH):iPTH and 3rd generation RIA

Secondary Outcome Measures

Parathyroid hormone carboxy terminal fragment levels PTH(7-84)
Ratio of PTH (1-84) to PTH (7-84)
Serum calcium level
Urine calcium level

Full Information

First Posted
February 6, 2006
Last Updated
December 18, 2018
Sponsor
Weill Medical College of Cornell University
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1. Study Identification

Unique Protocol Identification Number
NCT00288873
Brief Title
Characterization of Hyperparathyroidism and Vitamin D Deficiency in Obesity
Official Title
Characterization of Hyperparathyroidism and Vitamin D Deficiency in Obesity
Study Type
Interventional

2. Study Status

Record Verification Date
December 2018
Overall Recruitment Status
Completed
Study Start Date
February 2006 (undefined)
Primary Completion Date
July 2007 (Actual)
Study Completion Date
July 2007 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Weill Medical College of Cornell University

4. Oversight

5. Study Description

Brief Summary
Obese persons are known to have elevated levels of parathyroid hormone (PTH) and low levels of vitamin D. These hormones are important in regulation of the body's calcium stores and bone health. We would like to investigate these abnormalities and the accuracy of our current diagnostic tests by comparing results of standard assays for vitamin D and PTH to more specific tests, in obese subjects at baseline and as vitamin D is replaced. We will also compare two standard vitamin D replacement regimens to determine if one is more effective. This is a pilot study with two parts: Part 1 will compare levels of PTH and vitamin D using two different assays in obese subjects who have normal vitamin D and those who do not. We plan to enroll 20 subjects who have normal vitamin D levels and 40 subjects who have vitamin D insufficiency. All subjects will fill out questionnaires about the amount of calcium and vitamin D in their diet, and their recent sunlight exposure. We will ask for blood samples so that we can measure levels of calcium, vitamin D, albumin, creatinine, glucose, insulin and the different forms of PTH. Subjects who have vitamin D insufficiency will then be randomized to receive Vitamin D2 or Vitamin D3 in standard doses for eight weeks, in an open label trial. At four and eight weeks, these subjects will fill out the above questionnaires and have the blood tests repeated. For safety purposes, urine calcium will also be monitored.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vitamin D Deficiency, Secondary Hyperparathyroidism, Obesity
Keywords
Vitamin D deficiency, Secondary hyperparathyroidism, Obesity

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Ergocalciferol
Intervention Type
Drug
Intervention Name(s)
Cholecalciferol
Primary Outcome Measure Information:
Title
Vitamin D (25OHD):RIA and HPLC
Title
Parathyroid hormone (PTH):iPTH and 3rd generation RIA
Secondary Outcome Measure Information:
Title
Parathyroid hormone carboxy terminal fragment levels PTH(7-84)
Title
Ratio of PTH (1-84) to PTH (7-84)
Title
Serum calcium level
Title
Urine calcium level

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Obese subjects with body mass indices greater than 40 kg/m2 or 35 kg/m2 with other medical conditions secondary to obesity Willingness to take vitamin D supplements If baseline vitamin D level is >25 ng/ml subjects will be eligible for the control group If baseline vitamin D level is <25 ng/ml subjects will be eligible for one of the two vitamin D replacement groups Exclusion Criteria: Hypercalcemia Kidney disease Liver disease Malabsorption Prior diagnosis of bone disease Medical conditions requiring daily use of calcium, antacids, or medications known to affect bone metabolism or interact with vitamin D Hypersensitivity to any formulation of vitamin D
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Emily M Stein, M.D.
Organizational Affiliation
Weill Medical College of Cornell University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Weill Cornell Medical College
City
New York
State/Province
New York
ZIP/Postal Code
10021
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
19018785
Citation
Stein EM, Strain G, Sinha N, Ortiz D, Pomp A, Dakin G, McMahon DJ, Bockman R, Silverberg SJ. Vitamin D insufficiency prior to bariatric surgery: risk factors and a pilot treatment study. Clin Endocrinol (Oxf). 2009 Aug;71(2):176-83. doi: 10.1111/j.1365-2265.2008.03470.x. Epub 2008 Nov 5.
Results Reference
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Characterization of Hyperparathyroidism and Vitamin D Deficiency in Obesity

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