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Effect of Iron Reduction by Phlebotomy for Type 2 Diabetes

Primary Purpose

Type 2 Diabetes Mellitus, Prediabetes

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Phlebotomy
Sponsored by
University of Utah
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Type 2 Diabetes Mellitus focused on measuring iron, diabetes, phlebotomy

Eligibility Criteria

35 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 35-65
  • Prediabetes, or diabetes relatively well-controlled (Hemoglobin A1c [HbA1c] ≤ 8.0%) with a single oral agent as defined by oral glucose tolerance testing (OGTT) using criteria of the American Diabetes Association.
  • Serum ferritin values in the upper 50% of the normal range, 110-400 ng/mL for males, or 80-240 for females.

Exclusion Criteria:

  • hereditary hemochromatosis;
  • cancer (except cases currently with no evidence of disease);
  • serum creatinine >1.5;
  • anemia (Hgb < lower limit of normal);
  • chronic inflammatory conditions (rheumatologic conditions such as rheumatoid arthritis or giant cell arteritis, or chronic infections such as hepatitis B or C) that could affect ferritin;
  • erythrocyte sedimentation rate or C-reactive protein>1.5 times the upper limit of normal (UNL);
  • serum transaminases 2 x UNL;
  • hemophilia,
  • warfarin therapy,
  • history of GI bleeding;
  • current glucocorticoid therapy.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    No Intervention

    Arm Label

    Phlebotomy

    Control

    Arm Description

    All subjects receive counseling to follow a healthy diet and regular exercise. Phlebotomy occurs at the rate of 500 ml (one Unit) of blood per month over the period of 3-6 months. At two-month intervals, serum ferritin and complete blood counts are determined. When serum ferritin reaches the lowest quartile of normal (<50 ng/mL for females and <70 ng/mL for males, but no sooner than 3 months or later than 6 months after beginning phlebotomy, subjects will be retested for glucose tolerance as described

    Subjects receive counseling to follow a healthy diet and regular exercise.

    Outcomes

    Primary Outcome Measures

    Improvement in glucose area under the curve.
    As determined by oral glucose tolerance testing

    Secondary Outcome Measures

    Improvement in insulin sensitivity
    As determined by intravenous glucose tolerance testing
    Improvement in insulin secretory capacity
    As determined by intravenous glucose tolerance testing

    Full Information

    First Posted
    June 4, 2015
    Last Updated
    June 5, 2015
    Sponsor
    University of Utah
    Collaborators
    University of Colorado, Denver, University of New Mexico
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02468037
    Brief Title
    Effect of Iron Reduction by Phlebotomy for Type 2 Diabetes
    Official Title
    Iron Reduction by Phlebotomy for the Prevention and Treatment of Type 2 Diabetes
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    June 2015
    Overall Recruitment Status
    Completed
    Study Start Date
    April 2012 (undefined)
    Primary Completion Date
    May 2015 (Actual)
    Study Completion Date
    May 2015 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    University of Utah
    Collaborators
    University of Colorado, Denver, University of New Mexico

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    High tissue iron is a risk factor for diabetes even within the broad normal range of normal human values. In order to demonstrate the benefits of reducing iron on glucose homeostasis and to better define the parameters for larger clinical trials, the investigators will subject individuals with prediabetes (impaired glucose tolerance, IGT) or early type 2 diabetes to phlebotomy in order to reduce serum ferritin concentrations and determine the effect on glucose homeostasis as revealed by oral and frequently sampled intravenous glucose tolerance testing.
    Detailed Description
    Male and female subjects aged 35-65 will be recruited from the clinic populations at the Medical Centers of the Universities of Colorado, New Mexico, or Utah who have prediabetes, or diabetes relatively well-controlled (Hemoglobin A1c [HbA1c] ≤ 8.0%) with a single oral agent. Diabetes/prediabetes status is verified by oral glucose tolerance testing (OGTT) using criteria of the American Diabetes Association. Serum ferritin will be determined, and subjects chosen with values in the upper 50% of the normal range, 110-400 ng/mL for males, or 80-240 for females. Exclusion criteria include: hereditary hemochromatosis; cancer (except cases currently with no evidence of disease); serum creatinine >1.5; anemia (Hgb < lower limit of normal); chronic inflammatory conditions (rheumatologic conditions such as rheumatoid arthritis or giant cell arteritis, or chronic infections such as hepatitis B or C) that could affect ferritin; erythrocyte sedimentation rate or C-reactive protein>1.5 times the upper limit of normal (UNL); serum transaminases 2 x UNL; hemophilia, warfarin therapy, or history of GI bleeding; and current glucocorticoid therapy. After determination of eligibility, subjects are randomized in a 2:1 ratio for treatment and controls arms. In the fasted state, blood is drawn for determination of adiponectin and lipids (HDL, direct LDL, triglycerides). Subjects have the option of participating in a frequently sampled intravenous glucose tolerance test (FSIVGTT). All subjects receive counseling to follow a healthy diet and regular exercise. Phlebotomy occurs at the rate of 500 ml (one Unit) of blood per month over the period of 3-6 months. At two-month intervals, serum ferritin and complete blood counts are determined. When serum ferritin reaches the lowest quartile of normal (<50 ng/mL for females and <70 ng/mL for males, but no sooner than 3 months or later than 6 months after beginning phlebotomy, metabolic status will be reassessed by fasting lipids, adiponectin, OGTT, and optionally, FSIVGTT. Controls are recalled for repeat testing 6-8 months after enrollment. 120 min OGTT and FSIVGTT are performed on separate days after an overnight fast. FSIVGTT data are analyzed using MINMOD Millennium software. Areas under the glucose curve (AUCglucose) are calculated using the trapezoidal method.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Type 2 Diabetes Mellitus, Prediabetes
    Keywords
    iron, diabetes, phlebotomy

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    12 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Phlebotomy
    Arm Type
    Experimental
    Arm Description
    All subjects receive counseling to follow a healthy diet and regular exercise. Phlebotomy occurs at the rate of 500 ml (one Unit) of blood per month over the period of 3-6 months. At two-month intervals, serum ferritin and complete blood counts are determined. When serum ferritin reaches the lowest quartile of normal (<50 ng/mL for females and <70 ng/mL for males, but no sooner than 3 months or later than 6 months after beginning phlebotomy, subjects will be retested for glucose tolerance as described
    Arm Title
    Control
    Arm Type
    No Intervention
    Arm Description
    Subjects receive counseling to follow a healthy diet and regular exercise.
    Intervention Type
    Procedure
    Intervention Name(s)
    Phlebotomy
    Intervention Description
    Patients donate blood until tissue iron levels are in the lowest quartile of normal.
    Primary Outcome Measure Information:
    Title
    Improvement in glucose area under the curve.
    Description
    As determined by oral glucose tolerance testing
    Time Frame
    6 months after initiation of phlebotomy
    Secondary Outcome Measure Information:
    Title
    Improvement in insulin sensitivity
    Description
    As determined by intravenous glucose tolerance testing
    Time Frame
    6 months after initiation of phlebotomy
    Title
    Improvement in insulin secretory capacity
    Description
    As determined by intravenous glucose tolerance testing
    Time Frame
    6 months after initiation of phlebotomy

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    35 Years
    Maximum Age & Unit of Time
    65 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Age 35-65 Prediabetes, or diabetes relatively well-controlled (Hemoglobin A1c [HbA1c] ≤ 8.0%) with a single oral agent as defined by oral glucose tolerance testing (OGTT) using criteria of the American Diabetes Association. Serum ferritin values in the upper 50% of the normal range, 110-400 ng/mL for males, or 80-240 for females. Exclusion Criteria: hereditary hemochromatosis; cancer (except cases currently with no evidence of disease); serum creatinine >1.5; anemia (Hgb < lower limit of normal); chronic inflammatory conditions (rheumatologic conditions such as rheumatoid arthritis or giant cell arteritis, or chronic infections such as hepatitis B or C) that could affect ferritin; erythrocyte sedimentation rate or C-reactive protein>1.5 times the upper limit of normal (UNL); serum transaminases 2 x UNL; hemophilia, warfarin therapy, history of GI bleeding; current glucocorticoid therapy.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Donald McClain, MD, PhD
    Organizational Affiliation
    University of Utah
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

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