Semaglutide Anti-Atherosclerotic Mechanisms of Action Study in Type 2 Diabetes Patients (SAMAS)
Primary Purpose
Diabetes Mellitus, Type 2, Atherosclerosis
Status
Recruiting
Phase
Not Applicable
Locations
Slovenia
Study Type
Interventional
Intervention
Semaglutide Oral Tablet
Sponsored by
About this trial
This is an interventional treatment trial for Diabetes Mellitus, Type 2 focused on measuring semaglutide, atherosclerosis, diabetes mellitus type 2
Eligibility Criteria
Inclusion Criteria:
- type 2 diabetes
- therapy including at least metformin 1000 mg and sulphonyl urea at least half of the maximal dose
- BMI > or = 30 kg/m2
- HbA1c < or = 8,5%
- associated risk factors including smoking, dyslipidaemia, arterial hypertension, chronic kidney disease stage 1 to 3.
Exclusion Criteria:
- therapy with injectable GLP-1 receptor agonist ongoing or was taking place in the last year
- manifested cardiovascular disease
- heart failure
- chronic kidney disease stages 4 and 5
- advanced liver disease
- proliferative retinopathy or maculopathy
Sites / Locations
- UMC Ljubljana, Diabetes Outpatient ClinicRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
No Intervention
Arm Label
Interventional Arm
Comparative Arm
Arm Description
Beside metformin and sulphonyl urea treatment, the active, interventional arm, will be receiving Semaglutide Oral Tablets as per protocol, 3 mg for the first month, 7 mg in the second month and 14 mg form the third month onwards.
This group will not be receiving the additional therapy besides metformin and sulphonyl urea treatment. After 6 months a revaluation of glycemic control will be performed, if needed, rescue therapy with basal insulin will be implemented.
Outcomes
Primary Outcome Measures
Change in morphological arterial wall characteristics
Ultrasonographic assessment of cIMT (in millimetres)
Change in functional arterial wall characteristics
Endothelial function assessment by EndoPAT
Change in structural arterial wall characteristics
Arterial stiffness assessment by Sphygmocor device (in meters per second)
Secondary Outcome Measures
Change in atherogenic small dense low-density lipoproteins (sdLDL)
Assessment by gel electrophoresis
Change in glycated haemoglobin (HbA1c)
Assessment by biochemical methods
Change in high sensitivity C-reactive protein (hsCRP)
Assessment by biochemical methods
Correlations between changes in rate of cIMT reduction, % of endothelial function improvement and rate of arterial stiffness reduction on one hand and changes in concentration of sdLDL, % of HbA1c and concentration of hsCRP on the other
Statistical methods
Full Information
NCT ID
NCT05147896
First Posted
November 21, 2021
Last Updated
May 17, 2022
Sponsor
University Medical Centre Ljubljana
Collaborators
University of Palermo
1. Study Identification
Unique Protocol Identification Number
NCT05147896
Brief Title
Semaglutide Anti-Atherosclerotic Mechanisms of Action Study in Type 2 Diabetes Patients
Acronym
SAMAS
Official Title
Semaglutide Anti-Atherosclerotic Mechanisms of Action Study in Type 2 Diabetes Patients
Study Type
Interventional
2. Study Status
Record Verification Date
May 2022
Overall Recruitment Status
Recruiting
Study Start Date
May 1, 2022 (Actual)
Primary Completion Date
May 1, 2023 (Anticipated)
Study Completion Date
December 1, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Medical Centre Ljubljana
Collaborators
University of Palermo
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
Diabetes is a chronic disease characterized by chronic hyperglycaemia, causing microvascular and macrovascular complications. The latter lead to various disabilities: blindness, end-stage renal failure, nerve damage, formation of leg ulcers, and atherosclerosis. In people with type 2 diabetes, the probability of these atherosclerosis associated complications is twice as high as in people without diabetes. Cardiovascular diseases are also the main cause of mortality in people with diabetes.
Preventive measures are therefore crucial. In people with type 2 diabetes, in addition to good glycaemic control, the choice of antidiabetic drugs is also important. Large-scale research has shown that certain glucagon-like peptide (GLP-1) receptor agonists, in addition to improving the regulation of diabetes, also have a significant effect on reducing the macrovascular complications. It is now possible to use semaglutide, a GLP-1 receptor agonist, in the tablet form. Semaglutide lowers blood sugar only when the blood sugar value rises, due to food in the digestive tract, Thus, not increasing the risk of hypoglycaemia. In addition, semaglutide has a significant effect on weight loss and very beneficial, protective effects on the cardiovascular system. Large studies have shown that in its injectable form, it significantly reduces the incidence of cardiovascular death in patients with type 2 diabetes.
Therefore, the aim of the present study is to examine how semaglutide provides protective effects on the cardiovascular system and reduces the risk of diabetes type 2 associated complications.
The present study will include 100 people with type 2 diabetes and last for 12 months. The subjects will receive a semaglutide oral tablet daily in addition to their current treatment (combination of metformin and a sulphonyl urea). At the beginning of the study, after 6 months and at the end of the study (after 12 months of treatment), a detailed clinical examination will be performed and blood will be taken for laboratory parameters. In addition to basic blood tests, inflammatory and oxidative stress parameters, as well as lipid fractions parameters will also be assessed. Ultrasound examination of the changes in the carotid arteries and measures of additional properties of the arteries will also be performed. The confidentiality of the data of the participants in the research will be ensured, as the data obtained during the investigation will be encrypted before processing.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Type 2, Atherosclerosis
Keywords
semaglutide, atherosclerosis, diabetes mellitus type 2
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
100 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Interventional Arm
Arm Type
Active Comparator
Arm Description
Beside metformin and sulphonyl urea treatment, the active, interventional arm, will be receiving Semaglutide Oral Tablets as per protocol, 3 mg for the first month, 7 mg in the second month and 14 mg form the third month onwards.
Arm Title
Comparative Arm
Arm Type
No Intervention
Arm Description
This group will not be receiving the additional therapy besides metformin and sulphonyl urea treatment. After 6 months a revaluation of glycemic control will be performed, if needed, rescue therapy with basal insulin will be implemented.
Intervention Type
Drug
Intervention Name(s)
Semaglutide Oral Tablet
Other Intervention Name(s)
Rybelsus
Intervention Description
Semaglutide Oral Tablets will be introduced to the active arm as per protocol for regular therapy introduction.
Primary Outcome Measure Information:
Title
Change in morphological arterial wall characteristics
Description
Ultrasonographic assessment of cIMT (in millimetres)
Time Frame
1 year
Title
Change in functional arterial wall characteristics
Description
Endothelial function assessment by EndoPAT
Time Frame
1 year
Title
Change in structural arterial wall characteristics
Description
Arterial stiffness assessment by Sphygmocor device (in meters per second)
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Change in atherogenic small dense low-density lipoproteins (sdLDL)
Description
Assessment by gel electrophoresis
Time Frame
1 year
Title
Change in glycated haemoglobin (HbA1c)
Description
Assessment by biochemical methods
Time Frame
1 year
Title
Change in high sensitivity C-reactive protein (hsCRP)
Description
Assessment by biochemical methods
Time Frame
1 year
Title
Correlations between changes in rate of cIMT reduction, % of endothelial function improvement and rate of arterial stiffness reduction on one hand and changes in concentration of sdLDL, % of HbA1c and concentration of hsCRP on the other
Description
Statistical methods
Time Frame
1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
type 2 diabetes
therapy including at least metformin 1000 mg and sulphonyl urea at least half of the maximal dose
BMI > or = 30 kg/m2
HbA1c < or = 8,5%
associated risk factors including smoking, dyslipidaemia, arterial hypertension, chronic kidney disease stage 1 to 3.
Exclusion Criteria:
therapy with injectable GLP-1 receptor agonist ongoing or was taking place in the last year
manifested cardiovascular disease
heart failure
chronic kidney disease stages 4 and 5
advanced liver disease
proliferative retinopathy or maculopathy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Miodrag Janic, MD, PhD
Phone
+38640303383
Email
miodrag.janic@kclj.si
First Name & Middle Initial & Last Name or Official Title & Degree
Mojca Lunder, MD, PhD
Phone
+38641527618
Email
mojca.lunder@kclj.si
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Andrej Janež, Prof
Organizational Affiliation
University Medical Centre Ljubljana
Official's Role
Principal Investigator
Facility Information:
Facility Name
UMC Ljubljana, Diabetes Outpatient Clinic
City
Ljubljana
Country
Slovenia
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Miodrag Janic
Email
miodrag.janic@kclj.si
First Name & Middle Initial & Last Name & Degree
Mojca Lunder
Email
mojca.lunder@kclj.si
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
35258841
Citation
Janic M, Rizzo M, Cosentino F, Pantea Stoian A, Lunder M, Sabovic M, Janez A. Effect of Oral Semaglutide on Cardiovascular Parameters and Their Mechanisms in Patients with Type 2 Diabetes: Rationale and Design of the Semaglutide Anti-Atherosclerotic Mechanisms of Action Study (SAMAS). Diabetes Ther. 2022 Apr;13(4):795-810. doi: 10.1007/s13300-022-01226-y. Epub 2022 Mar 8.
Results Reference
derived
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Semaglutide Anti-Atherosclerotic Mechanisms of Action Study in Type 2 Diabetes Patients
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