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Do Aromatase Inhibitors (AIs) Decrease Intestinal Calcium Absorption?

Primary Purpose

Breast Cancer, Osteoporosis, Osteopenia

Status
Completed
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
Aromatase Inhibitor
Sponsored by
University of Wisconsin, Madison
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Breast Cancer

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Women at least 5 years past menopause, defined as date of last menses or bilateral oophorectomy
  • Newly diagnosed breast cancer and starting an AI as initial adjuvant therapy

Exclusion Criteria

  • Recent, current or planned chemotherapy for breast cancer, as this may have independent effects on intestinal health, calcium homeostasis and bone turnover
  • Allergy or intolerance to orange juice, as one isotope is given with orange juice
  • Current use of over-the-counter or prescription antacids, as they may influence Ca-Ab
  • Intestinal conditions associated with malabsorption or low gastric acid levels including Crohn's disease, ulcerative colitis, pernicious anemia, bacterial overgrowth, celiac sprue, chronic diarrhea or use of antibiotics within the past month
  • Known Stage 4 or 5 Chronic Kidney Disease, defined as an estimated GFR <30 cc/minute
  • Use of medications known to interfere with calcium or vitamin D metabolism, including oral steroids or anticonvulsants
  • Significant lymphedema precluding adequate intravenous access

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    aromatase inhibitor therapy

    Arm Description

    aromatase inhibitor therapy for six weeks

    Outcomes

    Primary Outcome Measures

    Change in Intestinal Calcium Absorption Related to Aromatase Inhibitor Therapy
    intestinal calcium absorption

    Secondary Outcome Measures

    Full Information

    First Posted
    October 2, 2008
    Last Updated
    September 13, 2012
    Sponsor
    University of Wisconsin, Madison
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00766532
    Brief Title
    Do Aromatase Inhibitors (AIs) Decrease Intestinal Calcium Absorption?
    Official Title
    Do Aromatase Inhibitors (AIs) Decrease Intestinal Calcium Absorption?
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    September 2012
    Overall Recruitment Status
    Completed
    Study Start Date
    January 2009 (undefined)
    Primary Completion Date
    October 2010 (Actual)
    Study Completion Date
    October 2010 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    University of Wisconsin, Madison

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    Research Question: Do Aromatase Inhibitors Decrease Intestinal Calcium Absorption? Study Design: Postmenopausal women with early stage breast cancer initiating aromatase inhibitor adjuvant therapy will participate in this two-month study. The primary study outcome is the change in intestinal calcium absorption following such therapy. Secondary outcomes are the changes in bone resorption markers and musculoskeletal signs and symptoms after initiation of therapy. We will interview women and review their medical records to determine eligibility. Eligible subjects will undergo two calcium absorption studies. The first study will determine their baseline calcium absorption, and the second study will occur after taking an aromatase inhibitor daily for at least 6 weeks. Women will present to the research unit in the early morning and receive an oral and intravenous stable calcium tracer with breakfast. Over the next 24 hours, we will collect all urine for measurement of its calcium content. During each inpatient stay, we will assess musculoskeletal symptoms by questionnaire and joint examination. Each woman will complete a four-day diet diary twice during the study.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Breast Cancer, Osteoporosis, Osteopenia, Fracture

    7. Study Design

    Primary Purpose
    Diagnostic
    Study Phase
    Phase 4
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    12 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    aromatase inhibitor therapy
    Arm Type
    Experimental
    Arm Description
    aromatase inhibitor therapy for six weeks
    Intervention Type
    Drug
    Intervention Name(s)
    Aromatase Inhibitor
    Intervention Description
    Any aromatase inhibitor started as initial adjuvant therapy
    Primary Outcome Measure Information:
    Title
    Change in Intestinal Calcium Absorption Related to Aromatase Inhibitor Therapy
    Description
    intestinal calcium absorption
    Time Frame
    baseline and 6 weeks later

    10. Eligibility

    Sex
    Female
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Women at least 5 years past menopause, defined as date of last menses or bilateral oophorectomy Newly diagnosed breast cancer and starting an AI as initial adjuvant therapy Exclusion Criteria Recent, current or planned chemotherapy for breast cancer, as this may have independent effects on intestinal health, calcium homeostasis and bone turnover Allergy or intolerance to orange juice, as one isotope is given with orange juice Current use of over-the-counter or prescription antacids, as they may influence Ca-Ab Intestinal conditions associated with malabsorption or low gastric acid levels including Crohn's disease, ulcerative colitis, pernicious anemia, bacterial overgrowth, celiac sprue, chronic diarrhea or use of antibiotics within the past month Known Stage 4 or 5 Chronic Kidney Disease, defined as an estimated GFR <30 cc/minute Use of medications known to interfere with calcium or vitamin D metabolism, including oral steroids or anticonvulsants Significant lymphedema precluding adequate intravenous access
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Karen E Hansen, MD
    Organizational Affiliation
    University of Wisconsin, Madison
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    22350731
    Citation
    Tevaarwerk A, Burkard ME, Wisinski KB, Shafer MM, Davis LA, Gogineni J, Crone E, Hansen KE. Aromatase inhibitors and calcium absorption in early stage breast cancer. Breast Cancer Res Treat. 2012 Jul;134(1):245-51. doi: 10.1007/s10549-012-1982-z. Epub 2012 Feb 18.
    Results Reference
    result

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