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Dapagliflozin vs Empagliflozin on Flow Mediated Dilation in Type 2 Diabetes Mellitus

Primary Purpose

Type 2 Diabetes Mellitus

Status
Unknown status
Phase
Phase 3
Locations
Mexico
Study Type
Interventional
Intervention
Dapagliflozin Pill
Empagliflozin Pill
Placebo pill
Sponsored by
Centro Universitario de Ciencias de la Salud, Mexico
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Type 2 Diabetes Mellitus focused on measuring Dapagliflozin, Empagliflozin, FMD, T2DM, Endothelial disfunction

Eligibility Criteria

40 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Diagnosis of T2DM
  • HbA1c > 7 y < 10
  • BMI 25 - 34.9 kg/m2
  • Signature of consent under information

Exclusion Criteria:

  • Hypertension
  • Treated with insulin and / or loop diuretics and thiazides
  • T1DM
  • Hypotension
  • With any autoimmune disease
  • Liver disease
  • Women who do not have a safe method of contraception
  • Women who are taking oral contraceptives or under treatment with hormone replacement therapy
  • Woman pregnant or breastfeeding
  • Untreated thyroid disease
  • Patients with a cardiovascular disease that contraindicates the use of this pharmacological class
  • Glomerular filtration rate <60ml/min (Cockcroft-Gault)

Sites / Locations

  • Institute of Experimental and Clinical Therapeutics (INTEC), CUCS, University of Guadalajara

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Placebo Comparator

Arm Label

Dapagliflozin

Empagliflozin

Placebo

Arm Description

Individuals with T2DM controlled with metformin; with no hypertension neither treated with insulin. Dapagliflozin capsules, 10 mg 1 time daily 5 minutes before the first meal

Individuals with T2DM controlled with metformin; with no hypertension neither treated with insulin. Empagliflozin capsules, 25 mg 1 time daily 5 minutes before the first meal

Individuals with T2DM controlled with metformin; with no hypertension neither treated with insulin. Dapagliflozin capsules, 400 mg 1 time daily 5 minutes before the first meal

Outcomes

Primary Outcome Measures

Flow Mediated Dilation
Change from baseline Flow mediated dilation at 7 days. Using a high-resolution UNEX EF38G ultrasound®, in a room at 22°C, with the patient lying supine, and the right arm extended

Secondary Outcome Measures

Fasting plasma glucose
Before and after intervention, using the BioSystems® Glucose Oxidase / Peroxidase kit; in an automated clinical chemistry analysis equipment brand XL-100Erba
Total cholesterol
Before and after intervention, using the BioSystems® Glucose Oxidase / Peroxidase kit.
Triglycerides
Before and after intervention, using the BioSystems® Glycerol phosphate Oxidase / Peroxidase kit.
High-density lipoprotein cholesterol
Before and after intervention, using the BioSystems® Direct / Detergent HDL kit
Low-density lipoprotein cholesterol
Before and after intervention using the BioSystems® Cholesterol Oxidase / Peroxidase kit
Creatinine
Before and after intervention the BioSystems® kit Modified Jaffe's no deproteinization
Blood pressure
Before and after intervention using an OMRON calibrated electronic digital sphygmomanometer model HEM 907 XL will be used. The patient will remain seated in a chair resting his back on the backrest, with a minimum rest of 5 minutes, The average of 3 measurements such as BP will be taken

Full Information

First Posted
December 4, 2019
Last Updated
December 10, 2019
Sponsor
Centro Universitario de Ciencias de la Salud, Mexico
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1. Study Identification

Unique Protocol Identification Number
NCT04195243
Brief Title
Dapagliflozin vs Empagliflozin on Flow Mediated Dilation in Type 2 Diabetes Mellitus
Official Title
Acute Effect of Dapagliflozin vs Empagliflozin Administration on Flow Mediated Dilation in Patients With Type 2 Diabetes Mellitus
Study Type
Interventional

2. Study Status

Record Verification Date
December 2019
Overall Recruitment Status
Unknown status
Study Start Date
December 2, 2019 (Anticipated)
Primary Completion Date
June 29, 2020 (Anticipated)
Study Completion Date
December 30, 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Centro Universitario de Ciencias de la Salud, Mexico

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
Type 2 diabetes mellitus (T2DM) is a considered one of the main global health challenges; the vascular endothelium plays an important role in vascular dysfunction in DM; Hyperglycemia induced by it is recognized as the main factor for the development of vascular complications of the disease, secondary to a reduction in nitric oxide production; "flow-mediated dilation" is the most commonly used technique for the evaluation of endothelial function, being the non-invasive method most widely used. It has been reported that with the use of SGLT2 inhibitors the development of cardiovascular complications in patients with T2DM is a decrease, as well the arterial stiffness, endothelial dysfunction and increasing on the shear stress and blood viscosity; and experimentally.
Detailed Description
The objective of this study, is to evaluate the acute effect of the administration of dapagliflozin in comparison with the administration of empagliflozin on endothelial disfunction in individuals with T2DM; we will conduct a double-blind, randomized, placebo-controlled, trial with 3 groups, each group of 24 male and female patients, between 40-65 years of age with T2DM, without hypertension, treated with insulins or thiazide diuretics. Randomization will determine who will receive the intervention during 7-days trial (Empagliflozin 25 mg 1 time daily 5 minutes or Dapagliflozin 10 mg before the first bite of each meal or approved placebo capsules), the patients will also continue with their usual treatment. The clinical findings and laboratory test and laboratory test include a metabolic profile and biosafety, baseline and at 7 days. Body weight, body fat, body mass index (BMI) and blood pressure will be determined during the initial and final visit, likewise, hemodynamics parameters of endothelial disfunction by flow mediate dilation with a high-resolution UNEX EF38G® ultrasound. Adverse events to treatment will be documented. Statistical analysis: Mann-Whitney U Test and Wilcoxon exact test. A p <0.05 will be considered statistically significant.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 2 Diabetes Mellitus
Keywords
Dapagliflozin, Empagliflozin, FMD, T2DM, Endothelial disfunction

7. Study Design

Primary Purpose
Other
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
24 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Dapagliflozin
Arm Type
Experimental
Arm Description
Individuals with T2DM controlled with metformin; with no hypertension neither treated with insulin. Dapagliflozin capsules, 10 mg 1 time daily 5 minutes before the first meal
Arm Title
Empagliflozin
Arm Type
Experimental
Arm Description
Individuals with T2DM controlled with metformin; with no hypertension neither treated with insulin. Empagliflozin capsules, 25 mg 1 time daily 5 minutes before the first meal
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Individuals with T2DM controlled with metformin; with no hypertension neither treated with insulin. Dapagliflozin capsules, 400 mg 1 time daily 5 minutes before the first meal
Intervention Type
Drug
Intervention Name(s)
Dapagliflozin Pill
Other Intervention Name(s)
Forxiga, Dapagliflozin
Intervention Description
The patient will take one pill, every 24 hr, during 7 days
Intervention Type
Drug
Intervention Name(s)
Empagliflozin Pill
Other Intervention Name(s)
Jardiance, Empagliflozin
Intervention Description
The patient will take one pill, every 24 hr, during 7 days
Intervention Type
Drug
Intervention Name(s)
Placebo pill
Other Intervention Name(s)
Calcined magnesia
Intervention Description
The patient will take one pill, every 24 hr, during 7 days
Primary Outcome Measure Information:
Title
Flow Mediated Dilation
Description
Change from baseline Flow mediated dilation at 7 days. Using a high-resolution UNEX EF38G ultrasound®, in a room at 22°C, with the patient lying supine, and the right arm extended
Time Frame
7 days
Secondary Outcome Measure Information:
Title
Fasting plasma glucose
Description
Before and after intervention, using the BioSystems® Glucose Oxidase / Peroxidase kit; in an automated clinical chemistry analysis equipment brand XL-100Erba
Time Frame
7 days
Title
Total cholesterol
Description
Before and after intervention, using the BioSystems® Glucose Oxidase / Peroxidase kit.
Time Frame
7 days
Title
Triglycerides
Description
Before and after intervention, using the BioSystems® Glycerol phosphate Oxidase / Peroxidase kit.
Time Frame
7 days
Title
High-density lipoprotein cholesterol
Description
Before and after intervention, using the BioSystems® Direct / Detergent HDL kit
Time Frame
7 days
Title
Low-density lipoprotein cholesterol
Description
Before and after intervention using the BioSystems® Cholesterol Oxidase / Peroxidase kit
Time Frame
7 days
Title
Creatinine
Description
Before and after intervention the BioSystems® kit Modified Jaffe's no deproteinization
Time Frame
7 days
Title
Blood pressure
Description
Before and after intervention using an OMRON calibrated electronic digital sphygmomanometer model HEM 907 XL will be used. The patient will remain seated in a chair resting his back on the backrest, with a minimum rest of 5 minutes, The average of 3 measurements such as BP will be taken
Time Frame
7 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of T2DM HbA1c > 7 y < 10 BMI 25 - 34.9 kg/m2 Signature of consent under information Exclusion Criteria: Hypertension Treated with insulin and / or loop diuretics and thiazides T1DM Hypotension With any autoimmune disease Liver disease Women who do not have a safe method of contraception Women who are taking oral contraceptives or under treatment with hormone replacement therapy Woman pregnant or breastfeeding Untreated thyroid disease Patients with a cardiovascular disease that contraindicates the use of this pharmacological class Glomerular filtration rate <60ml/min (Cockcroft-Gault)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Fernando Grover Paez, PhD
Phone
(33) 10585200
Ext
34215
Email
fgroverp@hotmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Fernando Grover Paez, PhD
Organizational Affiliation
Institute of Experimental and Clinical Therapeutics (INTEC), CUCS
Official's Role
Study Director
Facility Information:
Facility Name
Institute of Experimental and Clinical Therapeutics (INTEC), CUCS, University of Guadalajara
City
Guadalajara
State/Province
Jalisco
ZIP/Postal Code
44340
Country
Mexico
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Fernando Grover Paez, PhD
Phone
(33) 10585200
Ext
34215
Email
fgroverp@hotmail.com
First Name & Middle Initial & Last Name & Degree
Fernando Grover Paez, PhD
Phone
(33) 10585200
Ext
34215
Email
rballezaa@gmail.com

12. IPD Sharing Statement

Plan to Share IPD
No

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Dapagliflozin vs Empagliflozin on Flow Mediated Dilation in Type 2 Diabetes Mellitus

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