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Effects of Metformin in Heart Failure Patients

Primary Purpose

Type 2 Diabetes Mellitus

Status
Withdrawn
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Metformin
Subcutaneous (sliding scale) Insulin
Sponsored by
Maya Guglin
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Type 2 Diabetes Mellitus

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Patients > / = 18 years of age
  2. Admitted to the Medicine / Cardiology Advanced Heart Failure at UK Hospital
  3. Carry a diagnosis of heart failure with or without preserved ejection fraction
  4. Carry a diagnosis of type 2 diabetes mellitus

Exclusion Criteria:

  1. Patients <18 years of age
  2. Prisoners
  3. Terminal state
  4. Known adverse reaction or hypersensitivity to metformin administration
  5. Pregnancy
  6. Pathological conditions in which metformin administration is clinically contraindicated (Patients with acute or chronic metabolic acidosis, serum creatinine > 1.4 mg/dL in females, serum creatinine > 1.5 mg/dL in males)
  7. Patients with acute cardiovascular collapse, acute myocardial infarction, septicemia
  8. Patients carrying a diagnosis of type 1 diabetes mellitus
  9. Patients admitted with diabetic ketoacidosis or hyperosmotic hyperosmolar state.
  10. Patients who experience diabetic ketoacidosis or hyperosmotic hyperosmolar state at any point during their hospital admission.
  11. Patients admitted with a subcutaneous insulin pump
  12. Patients who, at the discretion of the Medicine / Cardiology Advanced Heart Failure service, required an endocrinology consult during their hospitalization where the endocrine consult service is opposed to utilizing metformin in a particular patient

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Other

    Other

    Arm Label

    Metformin

    Subcutaneous (sliding scale) Insulin

    Arm Description

    Continue Metformin while admitted to hospital

    Discontinue Metformin upon admission and be placed on sliding scale subcutaneous insulin treatment while admitted to hospital

    Outcomes

    Primary Outcome Measures

    Units of Insulin used
    doses and amounts on insulin needed

    Secondary Outcome Measures

    Blood glucose levels
    patient's glycemic control will be evaluated based on blood glucose levels
    Length of stay
    Lactate levels, mmol/L
    pro-BNP levels, pg/mL

    Full Information

    First Posted
    February 5, 2016
    Last Updated
    November 20, 2018
    Sponsor
    Maya Guglin
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02694289
    Brief Title
    Effects of Metformin in Heart Failure Patients
    Official Title
    Effects of Metformin in Heart Failure Patients
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    November 2018
    Overall Recruitment Status
    Withdrawn
    Why Stopped
    failure to enroll participants
    Study Start Date
    November 2016 (undefined)
    Primary Completion Date
    September 10, 2018 (Actual)
    Study Completion Date
    September 10, 2018 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor-Investigator
    Name of the Sponsor
    Maya Guglin

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    Hypothesis: In patients, who have diabetes type 2, are treated with metformin, and are admitted for HF, leads to reduced insulin requirements, as measured in units of insulin, with no negative impact on patient safety. This is a single center, prospective trial. Subjects will be randomized to initiate metformin (starting dose 500mg orally once daily up to a maximum dose of 2,500mg daily) OR be placed on insulin products for management of their type 2 diabetes mellitus.
    Detailed Description
    Because of the state of insulin resistance in heart failure (HF), metformin, with its ability to sensitize tissues to insulin, seems to be an ideal agent for managing type 2 diabetes mellitus (DM) in HF. It reduces the concentration of glucose in blood by enhancing insulin sensitivity, inducing greater peripheral uptake of glucose, and decreasing hepatic glucose output. However, according to the package insert, it is contraindicated in all patients with HF requiring pharmacologic treatment because of increased risk of lactic acidosis. The FDA has now de-escalated this contraindication to a warning as the evidence is lacking regarding an increased risk of lactic acidosis in patients with type 2 DM and HF who take metformin. Hypothesis: In patients, who have diabetes type 2, are treated with metformin, and are admitted for HF, metformin leads to reduced insulin requirements, as measured in units of insulin, with no negative impact on patient safety. Primary Objective: To test the hypothesis that continuing a patient's home metformin for diabetes management while admitted to UK hospital will result in decreased utilization of insulin as denoted by total units given. Secondary Objectives: To test the hypothesis that administering metformin in HF patients admitted to UK Hospital: Results in similar glycemic control (targeting a blood glucose < 200mg/dL) when compared with placebo along on the basis of basic metabolic panel glucose values. Both groups may receive conventional inpatient hyperglycemia management with insulin products Reduces drug and laboratory costs Reduces hospital length of stay Does not result in hypoglycemia (blood glucose < 60 mg/dL) Reduced discharge medication errors related to diabetic medications No observed increase in metabolic acidosis due to elevated lactate levels Does not impact heart failure status (as indicated by trending NT-pro BNP levels) Both the diagnosis and clinical management of patients with heart failure and type 2 diabetes mellitus will be guaranteed by the application of standard guidelines internationally recognized. All patients admitted to the Medicine / Cardiology Advanced Heart Failure at UK Hospital will be evaluated for inclusion and exclusion criteria. Based on our power analysis we plan to enroll 100 subjects total. Subjects will be enrolled from January 1, 2016 - December 31, 2018 until 120 patients are enrolled, estimated study time frame is two years.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Type 2 Diabetes Mellitus

    7. Study Design

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

    8. Arms, Groups, and Interventions

    Arm Title
    Metformin
    Arm Type
    Other
    Arm Description
    Continue Metformin while admitted to hospital
    Arm Title
    Subcutaneous (sliding scale) Insulin
    Arm Type
    Other
    Arm Description
    Discontinue Metformin upon admission and be placed on sliding scale subcutaneous insulin treatment while admitted to hospital
    Intervention Type
    Drug
    Intervention Name(s)
    Metformin
    Other Intervention Name(s)
    no other names
    Intervention Description
    Treatment/continuation of metformin therapy during admission
    Intervention Type
    Drug
    Intervention Name(s)
    Subcutaneous (sliding scale) Insulin
    Other Intervention Name(s)
    eg. Humulin, Lantus, Novalin
    Intervention Description
    Discontinue Metformin and be placed on subcutaneous sliding scale insulin during admission
    Primary Outcome Measure Information:
    Title
    Units of Insulin used
    Description
    doses and amounts on insulin needed
    Time Frame
    from time of hospital admission to hospital discharge, up to one year
    Secondary Outcome Measure Information:
    Title
    Blood glucose levels
    Description
    patient's glycemic control will be evaluated based on blood glucose levels
    Time Frame
    from time of hospital admission to hospital discharge, up to one year
    Title
    Length of stay
    Time Frame
    time from hospital admission to hospital discharge, up to one year
    Title
    Lactate levels, mmol/L
    Time Frame
    from time of hospital admission to hospital discharge, up to one year
    Title
    pro-BNP levels, pg/mL
    Time Frame
    from time of hospital admission to hospital discharge, up to one year

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Patients > / = 18 years of age Admitted to the Medicine / Cardiology Advanced Heart Failure at UK Hospital Carry a diagnosis of heart failure with or without preserved ejection fraction Carry a diagnosis of type 2 diabetes mellitus Exclusion Criteria: Patients <18 years of age Prisoners Terminal state Known adverse reaction or hypersensitivity to metformin administration Pregnancy Pathological conditions in which metformin administration is clinically contraindicated (Patients with acute or chronic metabolic acidosis, serum creatinine > 1.4 mg/dL in females, serum creatinine > 1.5 mg/dL in males) Patients with acute cardiovascular collapse, acute myocardial infarction, septicemia Patients carrying a diagnosis of type 1 diabetes mellitus Patients admitted with diabetic ketoacidosis or hyperosmotic hyperosmolar state. Patients who experience diabetic ketoacidosis or hyperosmotic hyperosmolar state at any point during their hospital admission. Patients admitted with a subcutaneous insulin pump Patients who, at the discretion of the Medicine / Cardiology Advanced Heart Failure service, required an endocrinology consult during their hospitalization where the endocrine consult service is opposed to utilizing metformin in a particular patient
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Maya Guglin, MD, PhD
    Organizational Affiliation
    University of Kentucky
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No

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    Effects of Metformin in Heart Failure Patients

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