Acute and Short-term Chronic Effects of Galvus (Vildagliptin) in Diabetes Type 2 Obese Women
Primary Purpose
1- Microvascular Function, 2-oxidative Stress, 3-inflammation
Status
Completed
Phase
Phase 4
Locations
Brazil
Study Type
Interventional
Intervention
Vildagliptin
Sponsored by

About this trial
This is an interventional treatment trial for 1- Microvascular Function focused on measuring endothelial function, microvascular function, incretins, diabetes mellitus, postprandial lipemia
Eligibility Criteria
Inclusion Criteria:
- All patients should have BMI > 30kg/m²
- Present untreated diabetes mellitus type 2
- Age between 19 and 50 years
- Waist Circumference > 80 cm
Exclusion Criteria:
- Renal, coronary vascular or peripheral, hematologic or hepatic disease
- Presence of severe hypertriglyceridemia (> 400mg/dl)
- Smokers
- Significant body mass loss (> 5%) within the six months prior to the study
Sites / Locations
- Laboratory for Clinical and Experimental Research on Vascular Biology
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
Metformin
Vildagliptina
Arm Description
Metformin 850mg/pill will be administered at lunch time and dinner time for 30 days
Vildagliptin 50mg/pill will be administered at 10 AM and at 6 PM also for 30 days.
Outcomes
Primary Outcome Measures
Change from Baseline in microcirculation function at 30 days
For this study, there will be used two methods, the traditional one, which consists in assessing the microcirculation parameters by dynamic nailfold videocapillaroscopy technique carried out in the nailfold pleat of the fourth finger on the left hand.
Secondary Outcome Measures
Change from Baseline in endothelial function at 30 days
LDF is a method for continuous non invasive determination of the microvascular perfusion, where the study of cutaneous vasomotion by spectral analysis of Laser Doppler signal allows the exploration of five frequency components: endothelial, myogenic, sympathetic, respiratory and cardiac, involved in answers to the stimuli. Therewith vasomotion during the whole study period will be assessed, to find differences in baseline, 30, 60, 120 and 180 min after the meal rich in lipids.
Full Information
NCT ID
NCT01827280
First Posted
April 2, 2013
Last Updated
May 30, 2017
Sponsor
Rio de Janeiro State University
Collaborators
Laboratory for Clinical and Experimental Research on Vascular Biology
1. Study Identification
Unique Protocol Identification Number
NCT01827280
Brief Title
Acute and Short-term Chronic Effects of Galvus (Vildagliptin) in Diabetes Type 2 Obese Women
Official Title
Acute and Short-term Chronic Effects of Galvus (Vildagliptin) on Endothelial Function and Oxidative Stress on Recently Diagnosed Type 2 Diabetic Obese Women: the Role of Intestinal Peptides During Lipid Overload
Study Type
Interventional
2. Study Status
Record Verification Date
May 2017
Overall Recruitment Status
Completed
Study Start Date
April 2013 (Actual)
Primary Completion Date
August 2016 (Actual)
Study Completion Date
November 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Rio de Janeiro State University
Collaborators
Laboratory for Clinical and Experimental Research on Vascular Biology
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The prevalence of obesity and type 2 diabetes mellitus (T2DM) has increased progressively in the past decades, and consequently, a higher incidence of cardiovascular diseases is observed. As this process develops, the endothelial dysfunction is present at early stages of the atherosclerotic disease. Studies conducted at BioVasc/UERJ show the occurrence of endothelial and microvascular dysfunction in obese carriers, even in the absence of dysglycemia. New concepts indicate the endothelium as a possible therapeutic target, and drugs which act not only on diabetes mellitus pathophysiology but also acting as direct cardiovascular protectors bring new therapeutic possibilities. The dipeptidyl-peptidase-4 inhibitors (DPP4), such as vildagliptin, are drugs used on the T2DM treatment. Its incretin mimetic and insulinotropic effects are already well established and several other studies show its effectiveness in reducing glycated hemoglobin, even in monotherapy.
Currently, fat rich foods are being increasingly introduced in the western way of life and recent evidence suggests that the postprandial lipemia (LPP) is related to cardiovascular risk. A better glucose control using vildagliptin can reduce the oxidative stress, and consequently promote a better microvascular and endothelial reactivity. However, vildagliptin can have an additional cardiovascular protective action, not only because of its effect on glycemia and oxidative stress reduction, but maybe because of its direct effect on intestinal peptides with postprandial lipemia reduction. To test this hypothesis, we will proceed the following exams: venous occlusion pletysmography, nailfold videocapilaroscopy and laser-Doppler flowmetry aiming to evaluate vascular reactivity on muscle and at cutaneous site. Anoter group of patients with the same clinical charactherisitics will use metformin, in order to compare its effects with those obtained from the use of Vildaglitpin. Our purpose is to determine whether vildagliptin, evaluated in obese and diabetic women, has vascular protective effects, and whether the regulatory mechanisms of these actions correlate with oxidative stress, inflammatory markers and intestinal peptides in baseline state and after a lipid overload.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
1- Microvascular Function, 2-oxidative Stress, 3-inflammation
Keywords
endothelial function, microvascular function, incretins, diabetes mellitus, postprandial lipemia
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
40 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Metformin
Arm Type
Experimental
Arm Description
Metformin 850mg/pill will be administered at lunch time and dinner time for 30 days
Arm Title
Vildagliptina
Arm Type
Experimental
Arm Description
Vildagliptin 50mg/pill will be administered at 10 AM and at 6 PM also for 30 days.
Intervention Type
Drug
Intervention Name(s)
Vildagliptin
Other Intervention Name(s)
Vildagliptin (galvus)
Intervention Description
Vildagliptin 50mg/pill will be administered at 10 AM and at 6 PM also for 30 days.
Primary Outcome Measure Information:
Title
Change from Baseline in microcirculation function at 30 days
Description
For this study, there will be used two methods, the traditional one, which consists in assessing the microcirculation parameters by dynamic nailfold videocapillaroscopy technique carried out in the nailfold pleat of the fourth finger on the left hand.
Time Frame
Before and after 30 days
Secondary Outcome Measure Information:
Title
Change from Baseline in endothelial function at 30 days
Description
LDF is a method for continuous non invasive determination of the microvascular perfusion, where the study of cutaneous vasomotion by spectral analysis of Laser Doppler signal allows the exploration of five frequency components: endothelial, myogenic, sympathetic, respiratory and cardiac, involved in answers to the stimuli. Therewith vasomotion during the whole study period will be assessed, to find differences in baseline, 30, 60, 120 and 180 min after the meal rich in lipids.
Time Frame
before and after 30 days (intervention)
Other Pre-specified Outcome Measures:
Title
Change from Baseline in incretins and inflammation markers at 30 days
Description
Through kits read by Multiplex® appliance, inflammatory markers will be evaluated, all simultaneously, with small sample quantity (from 10 to 50µL).
Time Frame
basal and after 30 days (intervention)
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
19 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
All patients should have BMI > 30kg/m²
Present untreated diabetes mellitus type 2
Age between 19 and 50 years
Waist Circumference > 80 cm
Exclusion Criteria:
Renal, coronary vascular or peripheral, hematologic or hepatic disease
Presence of severe hypertriglyceridemia (> 400mg/dl)
Smokers
Significant body mass loss (> 5%) within the six months prior to the study
Facility Information:
Facility Name
Laboratory for Clinical and Experimental Research on Vascular Biology
City
Rio de Janeiro
ZIP/Postal Code
20550-900
Country
Brazil
12. IPD Sharing Statement
Citations:
PubMed Identifier
31462933
Citation
Schiapaccassa A, Maranhao PA, de Souza MDGC, Panazzolo DG, Nogueira Neto JF, Bouskela E, Kraemer-Aguiar LG. 30-days effects of vildagliptin on vascular function, plasma viscosity, inflammation, oxidative stress, and intestinal peptides on drug-naive women with diabetes and obesity: a randomized head-to-head metformin-controlled study. Diabetol Metab Syndr. 2019 Aug 23;11:70. doi: 10.1186/s13098-019-0466-2. eCollection 2019.
Results Reference
derived
Learn more about this trial
Acute and Short-term Chronic Effects of Galvus (Vildagliptin) in Diabetes Type 2 Obese Women
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