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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
Baskent University
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional prevention trial for Type 2 Diabetes Mellitus

Eligibility Criteria

45 Years - undefined (Adult, Older Adult)FemaleAccepts Healthy Volunteers

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

    First Posted
    February 26, 2007
    Last Updated
    February 26, 2007
    Sponsor
    Baskent University
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    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

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    Effects of Rosiglitazone on Bone in Postmenopausal Diabetic Women

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