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Withdrawn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

About this trial
This is an interventional treatment trial for Type 2 Diabetes Mellitus
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
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
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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