Effects of Rosiglitazone on Bone in Postmenopausal Diabetic Women
Primary Purpose
Type 2 Diabetes Mellitus, Obesity, Menopause
Status
Completed
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
Rosiglitazone
Sponsored by

About this trial
This is an interventional prevention trial for Type 2 Diabetes Mellitus
Eligibility Criteria
Inclusion Criteria:
- Newly diagnosed type 2 diabetes mellitus
- Postmenopausal period
Exclusion Criteria:
- Recent fracture or osteoporosis
- Drugs that may affect calcium or bone metabolism or drugs known to interfere with cytokine release
- Thyroid, parathyroid, pituitary, nutritional, inflammatory, hepatic, renal, or neoplastic disorders
- Severe cardiovascular disease
Sites / Locations
Outcomes
Primary Outcome Measures
metabolic bone markers before and after the intervention,
Secondary Outcome Measures
association between the changes in bone turnover parameters and plasma cytokine levels
Full Information
NCT ID
NCT00440375
First Posted
February 26, 2007
Last Updated
February 26, 2007
Sponsor
Baskent University
1. Study Identification
Unique Protocol Identification Number
NCT00440375
Brief Title
Effects of Rosiglitazone on Bone in Postmenopausal Diabetic Women
Study Type
Interventional
2. Study Status
Record Verification Date
February 2007
Overall Recruitment Status
Completed
Study Start Date
June 2005 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
March 2006 (undefined)
3. Sponsor/Collaborators
Name of the Sponsor
Baskent University
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to evaluate the effect of rosiglitazone on bone metabolism and to assess the association between the changes in bone turnover parameters and plasma cytokine levels in postmenopausal diabetic women
Detailed Description
Fifty-six obese, drug naive patients with type 2 diabetes mellitus were enrolled and completed the study. Twenty-six healthy subjects matched for age and body mass index (BMI) served as nondiabetic controls. All subjects were postmenopausal women with last menses at least 2 years. After the baseline measurements, all subjects were instructed to follow a weight-maintaining diet, based on ADA recommendations, and were also encouraged to walk or to jog at least 30 min daily. Subsequently, 28 of the diabetic subjects were randomly assigned to receive rosiglitazone (4 mg/day). Twenty-eight of diabetic subjects were on diet alone. The randomization procedure was based on a random sequence.
All subjects had a complete clinical examination, anthropometric measurements, and laboratory tests at baseline and at the end of the 12th week of the study. Laboratory investigations included assessment of: (i) glycemic control (HbA1c, fasting plasma glucose and insulin levels, and homeostasis model assessment (HOMA) index (22); (ii) serum bsALP and active human osteocalcin concentration (OCL) as markers of bone formation; (iii) urine deoxypyridinoline (DPD) as marker of bone resorption. Other non-specific bone markers including serum total ALP activity, urinary calcium (Ca) and phosphate (PO4) concentrations were also measured. Urine concentrations of DPD (nmol/L), Ca and PO4 (both in mmol/L) were corrected for their respective urine creatinine (Cr) concentrations in mmol/L (Urine DPD/Cr, Urine Ca/Cr and Urine PO4/Cr respectively). In addition, fasting blood samples were analyzed for plasma cytokine levels including IL-1β, IL-6 and TNF-α, and for haptoglobin levels.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 2 Diabetes Mellitus, Obesity, Menopause
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
82 (false)
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
Rosiglitazone
Primary Outcome Measure Information:
Title
metabolic bone markers before and after the intervention,
Secondary Outcome Measure Information:
Title
association between the changes in bone turnover parameters and plasma cytokine levels
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Newly diagnosed type 2 diabetes mellitus
Postmenopausal period
Exclusion Criteria:
Recent fracture or osteoporosis
Drugs that may affect calcium or bone metabolism or drugs known to interfere with cytokine release
Thyroid, parathyroid, pituitary, nutritional, inflammatory, hepatic, renal, or neoplastic disorders
Severe cardiovascular disease
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Zehra Berberoglu
Organizational Affiliation
The Society of Endocrinology and Metabolism of Turkey
Official's Role
Principal Investigator
12. IPD Sharing Statement
Citations:
PubMed Identifier
17595249
Citation
Berberoglu Z, Gursoy A, Bayraktar N, Yazici AC, Bascil Tutuncu N, Guvener Demirag N. Rosiglitazone decreases serum bone-specific alkaline phosphatase activity in postmenopausal diabetic women. J Clin Endocrinol Metab. 2007 Sep;92(9):3523-30. doi: 10.1210/jc.2007-0431. Epub 2007 Jun 26.
Results Reference
derived
Learn more about this trial
Effects of Rosiglitazone on Bone in Postmenopausal Diabetic Women
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