The Effects of Empagliflozin on Arterial Wall Characteristics
Primary Purpose
Vascular Stiffness, Hypoglycemic Agents, Diabetes Complications
Status
Unknown status
Phase
Phase 4
Locations
Slovenia
Study Type
Interventional
Intervention
Empagliflozin 25mg
Metformin
Empagliflozin/Metformin
Placebos
Sponsored by
About this trial
This is an interventional treatment trial for Vascular Stiffness
Eligibility Criteria
Inclusion Criteria:
- diabetes mellitus type 1
Exclusion Criteria:
- diagnosed advanced heart, kidney or liver failure
- benign prostatic hyperplasia
- prostatic carcinoma
- frequent urinary tract infections
- non-type 1 diabetes mellitus
Sites / Locations
- University Medical Centre LjubljanaRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm Type
Active Comparator
Active Comparator
Active Comparator
Placebo Comparator
Arm Label
*empagliflozin*
*metformin*
*empagliflozin/metformin*
*placebo*
Arm Description
empagliflozin 25 mg daily for 12 weeks, once daily, by mouth
metformin 2000 mg daily for 12 weeks, once daily, by mouth
empagliflozin 25 mg daily and metformin 2000 mg daily for 12 weeks, by mouth
placebo for 12 weeks, once daily with water, by mouth
Outcomes
Primary Outcome Measures
Arterial function
Endothelial function and arterial stiffness will be measured.
Secondary Outcome Measures
Glycemic control
HbA1c will be measured.
Full Information
NCT ID
NCT03639545
First Posted
August 10, 2018
Last Updated
August 18, 2018
Sponsor
University Medical Centre Ljubljana
1. Study Identification
Unique Protocol Identification Number
NCT03639545
Brief Title
The Effects of Empagliflozin on Arterial Wall Characteristics
Official Title
The Effects of Empagliflozin on Functional and Structural Arterial Wall Characteristics
Study Type
Interventional
2. Study Status
Record Verification Date
August 2018
Overall Recruitment Status
Unknown status
Study Start Date
March 1, 2018 (Actual)
Primary Completion Date
December 30, 2018 (Anticipated)
Study Completion Date
January 30, 2019 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Medical Centre Ljubljana
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Introduction: Diabetes mellitus is characterized by impaired arterial function and high incidence of cardiovascular events. Metformin and most recent antidiabetic groups of drugs, SGLT2 inhibitors, were in previous studies shown to reduce cardiovascular events. Until now, direct effect of empagliflozin on arterial function and its comparison to metformin was not studied yet.
Aim: The aim of the present study is to explore and compare potential direct effects of empagliflozin and metformin on arterial functional and structural arterial wall characteristics in patients with type 1 diabetes mellitus.
Methods: Patients with type 1 diabetes mellitus are randomized into four groups: 1) empagliflozin (25 mg daily), 2) metformin (2000 mg daily), 3) combination (empagliflozin 25 mg daily and metformin 2000 mg daily) and 4) control (placebo). At inclusion and after 12 weeks treatment, arterial function is assessed: endothelial function (brachial artery flow-mediated dilation (FMD), reactive hyperemia index (RHI)) and arterial stiffness (carotid pulse wave velocity (PWV), carotid-femoral PWV (cfPWV) and common carotid artery stiffness (β-stiffness)).
Detailed Description
Introduction: Diabetes mellitus is characterized by impaired arterial function and high incidence of cardiovascular events. Metformin and most recent antidiabetic groups of drugs, SGLT2 inhibitors, were in previous studies shown to reduce cardiovascular events. Until now, direct effect of empagliflozin on arterial function and its comparison to metformin was not studied yet.
Aim: The aim of the present study is to explore and compare potential direct effects of empagliflozin and metformin on arterial functional and structural arterial wall characteristics in patients with type 1 diabetes mellitus.
Methods: Patients with type 1 diabetes mellitus are randomized into four groups: 1) empagliflozin (25 mg daily), 2) metformin (2000 mg daily), 3) combination (empagliflozin 25 mg daily and metformin 2000 mg daily) and 4) control (placebo). At inclusion and after 12 weeks treatment, arterial function is assessed: endothelial function (brachial artery flow-mediated dilation (FMD), reactive hyperemia index (RHI)) and arterial stiffness (carotid pulse wave velocity (PWV), carotid-femoral PWV (cfPWV) and common carotid artery stiffness (β-stiffness)).
Background:
Diabetes mellitus is characterized by chronic hyperglycaemia causing chronic microvascular and macrovascular complications. Among the microvascular complications, diabetic retinopathy, neuropathy and nephropathy are included. Macrovascular complications include atherosclerotic brain-vascular disease, coronary disease and peripheral arterial disease. Chronic complications of diabetes pose a greater risk of disability, development of blindness, renal failure, neuropathy and cardiovascular disease. Consequently, a good glycemic control is crucial to protect the patients from the development of chronic complications. In this regard, glycemic control is of primary importance, as well as the choice of treatment that can further improve the functioning of the arteries and thus protect against the onset of cardiovascular damage or complications.
For the treatment of hyperglycemia patients with type 1 diabetes need insulin. Some oral anti-diabetics have been found to improve glycemic control, reduce insulin consumption (the total daily insulin dose), and also protect against the development of cardiovascular complications. Such effects have been shown in clinical studies for metformin. The latter improved from endothelium-dependent relaxation of the arteries and reduced insulin resistance, but most studies were performed in patients with type 2 diabetes and studies in type 1 diabetes are limited.
A novel group of oral antidiabetics are SGLT2 inhibitors, such as empagliflozin, reduce glucose reabsorption in proximal kidney tubules and increase glucose excretion through urine. Most of the previous studies on the efficacy of empagliflozin basic antidiabetic activity and additional effects have been performed in patients with type 2 diabetes. They were shown to improve glyceamia control and also reduced blood pressure body weight. In patients with type 1 diabetes, favorable effects of empagliflozin on the reduction of arterial wall stiffness and blood pressure reduction were observed, but no systematic studies were performed yet and the mechanisms behind the beneficial effects are not known yet.
Methods:
Type 1 diabetes mellitus patients are being recruited. The patients are equally randomized into 4 groups that receive one of the three drugs in addition to insulin. The groups were as follows: 1) empagliflozin group (receiving 25 mg daily), 2) metformin group (receiving 2000 mg daily), combination group (receiving empagliflozin 25 mg daily and metformin 2000 mg daily) and 4) control group (receiving placebo). The duration of the study period is 12 weeks. All subjects are voluntarily participating in this study. The study was approved by the National Medical Ethics Committee of Slovenia.
At the beginning of the study, a complete history and full medical examination of each patient are performed. At inclusion to the study and after 12 weeks of treatment, arterial function measurements are performed, comprising of i) measurements of endothelial function (brachial artery flow-mediated dilation (FMD), reactive hyperemia index (RHI)); and ii) measurements of arterial stiffness (carotid artery pulse wave velocity (PWV), carotid-femoral PWV (cfPWV) and common carotid artery stiffness (β-stiffness)). Additionally, venous blood samples are obtained at the beginning and at the end of the study period. Automated sphygmomanometer is used for blood pressure measurements. Ultrasound measurements are obtained on Aloka ProSound alpha7 machine with integrated high resolution eTracking system. Endothelial function, by means of brachial artery FMD, was assessed in accordance to the current guidelines. Reactive hyperemia index is measured using Endopat 2000 device (Itamar Medical Ltd., Caesarea, Israel), while cfPWV is obtained using SphygmoCor device (AtCor Medical, Sydney, Australia) with SphygmoCor CvMS software (version 9).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vascular Stiffness, Hypoglycemic Agents, Diabetes Complications, Diabetes Mellitus, Type 1
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
120 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
*empagliflozin*
Arm Type
Active Comparator
Arm Description
empagliflozin 25 mg daily for 12 weeks, once daily, by mouth
Arm Title
*metformin*
Arm Type
Active Comparator
Arm Description
metformin 2000 mg daily for 12 weeks, once daily, by mouth
Arm Title
*empagliflozin/metformin*
Arm Type
Active Comparator
Arm Description
empagliflozin 25 mg daily and metformin 2000 mg daily for 12 weeks, by mouth
Arm Title
*placebo*
Arm Type
Placebo Comparator
Arm Description
placebo for 12 weeks, once daily with water, by mouth
Intervention Type
Drug
Intervention Name(s)
Empagliflozin 25mg
Other Intervention Name(s)
empagliflozin
Intervention Description
The patients receive empagliflozin (25 mg daily) for 12 weeks.
Intervention Type
Drug
Intervention Name(s)
Metformin
Intervention Description
The patients receive metformin (2000 mg daily) for 12 weeks.
Intervention Type
Drug
Intervention Name(s)
Empagliflozin/Metformin
Other Intervention Name(s)
empagliflozin and metformin
Intervention Description
The patients receive empagliflozin 25 mg daily and metformin 2000 mg daily or placebo for 12 weeks.
Intervention Type
Drug
Intervention Name(s)
Placebos
Other Intervention Name(s)
placebo
Intervention Description
The patients receive for 12 weeks.
Primary Outcome Measure Information:
Title
Arterial function
Description
Endothelial function and arterial stiffness will be measured.
Time Frame
the change of arterial function from baseline to 12 weeks of treatment
Secondary Outcome Measure Information:
Title
Glycemic control
Description
HbA1c will be measured.
Time Frame
the change of HbA1c from baseline to 12 weeks of treatment
10. Eligibility
Sex
All
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
diabetes mellitus type 1
Exclusion Criteria:
diagnosed advanced heart, kidney or liver failure
benign prostatic hyperplasia
prostatic carcinoma
frequent urinary tract infections
non-type 1 diabetes mellitus
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Mojca Lunder, MD, PhD
Phone
+38615223140
Email
mojca.lunder@kclj.si
First Name & Middle Initial & Last Name or Official Title & Degree
Miodrag Janic, MD, PhD
Phone
+38615228012
Email
miodrag.janic@kclj.si
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Andrej Janez, prof
Organizational Affiliation
University Medical Centre Ljubljana
Official's Role
Study Chair
Facility Information:
Facility Name
University Medical Centre Ljubljana
City
Ljubljana
ZIP/Postal Code
SI-1000
Country
Slovenia
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mojca Lunder, MD, PhD
Phone
+386 1 5223140
Email
mojca.lunder@kclj.si
First Name & Middle Initial & Last Name & Degree
Andrej Janez, Prof
Phone
+386 1 5223564
Email
andrej.janez@kclj.si
First Name & Middle Initial & Last Name & Degree
Miodrag Janic, MD, PhD
First Name & Middle Initial & Last Name & Degree
Miso Sabovic, Prof
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
30509271
Citation
Lunder M, Janic M, Japelj M, Juretic A, Janez A, Sabovic M. Empagliflozin on top of metformin treatment improves arterial function in patients with type 1 diabetes mellitus. Cardiovasc Diabetol. 2018 Dec 3;17(1):153. doi: 10.1186/s12933-018-0797-6.
Results Reference
derived
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The Effects of Empagliflozin on Arterial Wall Characteristics
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