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Effects of SGLT2 Inhibitor on Hemodynamic Parameters in Resistant Hypertensive Subjects

Primary Purpose

Hypertension, Diabetes Mellitus, Type 2, Blood Pressure

Status
Completed
Phase
Phase 4
Locations
Brazil
Study Type
Interventional
Intervention
Dapagliflozin 10mg
Glibenclamide 5Mg Tablet
Sponsored by
University of Campinas, Brazil
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hypertension

Eligibility Criteria

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

Inclusion Criteria:

  • Resistant hypertension and type 2 diabetes diagnoses after a 6-month follow-up
  • Use of metformin therapy
  • Therapy adherence
  • Agree to participate in the research protocol and sign the informed consent form

Exclusion Criteria:

  • secondary Hypertension
  • pseudoresistance hypertension (poor medication adherence and white coat hypertension)
  • patients with symptomatic ischemic heart disease, impaired renal function, liver disease and history of stroke, myocardial infarction and peripheral vascular diseases
  • pregnancy
  • smoking
  • autoimmune diseases

Sites / Locations

  • University of Campinas (UNICAMP)

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Dapagliflozin

Glibenclamide

Arm Description

Dapagliflozin 10mg daily for 12 weeks.

Glibenclamide 5mg daily for 12 weeks.

Outcomes

Primary Outcome Measures

Change in Systolic Blood Pressure
Change in Office Systolic Blood Pressure after 12 weeks of treatment

Secondary Outcome Measures

Change in Ambulatory Systolic Blood Pressure
Change in Ambulatory Systolic Blood Pressure after 12 weeks of treatment
Change in weight
Change in body weight
Change in arterial stiffness
Change in arterial stiffness measured by Sphygmocor device
Change in left ventricular hypertrophy
Change in left ventricular hypertrophy measured by Echocardiogram
Change in microalbuminuria
Change in microalbuminuria measured by Urine Albumin/Creatinine Ratio

Full Information

First Posted
March 20, 2017
Last Updated
May 2, 2018
Sponsor
University of Campinas, Brazil
Collaborators
Fundação de Amparo à Pesquisa do Estado de São Paulo
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1. Study Identification

Unique Protocol Identification Number
NCT03089333
Brief Title
Effects of SGLT2 Inhibitor on Hemodynamic Parameters in Resistant Hypertensive Subjects
Official Title
Effects of Dapagliflozin, an SGLT2 Inhibitor, on Hemodynamic Parameters, Target Organ Damage and Obesity Profile in Resistant Hypertensive Subjects
Study Type
Interventional

2. Study Status

Record Verification Date
May 2018
Overall Recruitment Status
Completed
Study Start Date
July 2016 (Actual)
Primary Completion Date
October 2017 (Actual)
Study Completion Date
December 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Campinas, Brazil
Collaborators
Fundação de Amparo à Pesquisa do Estado de São Paulo

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
New strategies trying to achieve blood pressure control and consequently reduce cardiovascular risk in resistant hypertensive subjects are promising. In this context, the SGLT2 inhibitor dapagliflozin, not yet investigated in resistant hypertension, arises as a potential drug in order to impact on blood pressure levels, as well as target organ damage and adiposity in this high-risk population.
Detailed Description
Objective: The investigators aim to assess whether the intervention with the SGLT2 inhibitor -dapaglifozin - reduces PA levels, target organ damage, fat profile and change the adipokines levels in patients with resistant hypertension with DM2. Methods and design: This crossover randomized, double-blind, interventional study controlled by standard therapy will include 20 patients with resistant hypertension and type 2 diabetes, followed in Outpatient Clinic specialized in Resistant Hypertension at clinical Hospital-UNICAMP. They will be randomly assigned into two groups (1) initially treated with dapagliflozin in combination with their usual antihypertensive therapy and metformin, at 12 weeks (n = 10) or group (2) Control initially treated with glibenclamide at a dose of 5mg daily in combination with antihypertensive therapy usual and metformin, at 12 weeks (n = 10). Office ambulatory and home BP measurements; anthropometric measurements, determination of vascular stiffness by pulse wave velocity, echocardiogram, body bioimpedance, enzyme immunoassays for the determination of adipokines, and lab tests to evaluate biochemical parameters will be performed pre- and after the use of both treatments. Glycemic parameters, and weight will be assessed every 4 weeks. Results and conclusion: The use of SGLT2 inhibitor in these patients may provide new strategies for treatment of patients with resistant hypertension.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypertension, Diabetes Mellitus, Type 2, Blood Pressure, Obesity, Cardiac Hypertrophy, Microalbuminuria, Vascular Stiffness

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Model Description
Two-way crossover design
Masking
Investigator
Allocation
Randomized
Enrollment
16 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Dapagliflozin
Arm Type
Experimental
Arm Description
Dapagliflozin 10mg daily for 12 weeks.
Arm Title
Glibenclamide
Arm Type
Active Comparator
Arm Description
Glibenclamide 5mg daily for 12 weeks.
Intervention Type
Drug
Intervention Name(s)
Dapagliflozin 10mg
Other Intervention Name(s)
FARXIGA®
Intervention Description
Dapagliflozin at a dose of 10mg daily in combination with metoformin and current antihypertensive therapy for 12 weeks
Intervention Type
Drug
Intervention Name(s)
Glibenclamide 5Mg Tablet
Other Intervention Name(s)
Glibenclamide
Intervention Description
Glibenclamide at a dose of 5mg daily in combination with metoformin and current antihypertensive therapy for 12 weeks
Primary Outcome Measure Information:
Title
Change in Systolic Blood Pressure
Description
Change in Office Systolic Blood Pressure after 12 weeks of treatment
Time Frame
Baseline and 12 weeks
Secondary Outcome Measure Information:
Title
Change in Ambulatory Systolic Blood Pressure
Description
Change in Ambulatory Systolic Blood Pressure after 12 weeks of treatment
Time Frame
Baseline and 12 weeks
Title
Change in weight
Description
Change in body weight
Time Frame
Baseline and 12 weeks
Title
Change in arterial stiffness
Description
Change in arterial stiffness measured by Sphygmocor device
Time Frame
Baseline and 12 weeks
Title
Change in left ventricular hypertrophy
Description
Change in left ventricular hypertrophy measured by Echocardiogram
Time Frame
Baseline and 12 weeks
Title
Change in microalbuminuria
Description
Change in microalbuminuria measured by Urine Albumin/Creatinine Ratio
Time Frame
Baseline and 12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Resistant hypertension and type 2 diabetes diagnoses after a 6-month follow-up Use of metformin therapy Therapy adherence Agree to participate in the research protocol and sign the informed consent form Exclusion Criteria: secondary Hypertension pseudoresistance hypertension (poor medication adherence and white coat hypertension) patients with symptomatic ischemic heart disease, impaired renal function, liver disease and history of stroke, myocardial infarction and peripheral vascular diseases pregnancy smoking autoimmune diseases
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rodrigo Modolo, MD, PhD
Organizational Affiliation
University of Campinas
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Campinas (UNICAMP)
City
Campinas
State/Province
São Paulo
ZIP/Postal Code
13083970
Country
Brazil

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Effects of SGLT2 Inhibitor on Hemodynamic Parameters in Resistant Hypertensive Subjects

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