Back to results

Short-term Effects of Dapagliflozin on Peak VO2 in HFrEF (DAPA-VO2)

Primary Purpose

Heart Failure With Reduced Ejection Fraction

Status

Completed

Phase

Phase 4

Locations

Spain

Study Type

Interventional

Intervention

Maximal functional capacity by cardiopulmonary exercise testing

Echocardiography

Evaluation of health related quality of life

Submáximal functional capacity assesment by 6 minutes walk test

Clinical evaluation

About this trial

This is an interventional treatment trial for Heart Failure With Reduced Ejection Fraction focused on measuring Heart Failure with Reduced Ejection Fraction, Functional Capacity, Quality of life

Eligibility Criteria

18 Years - 99 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

The participant or his legal representative is willing and able to give informed consent for participation in the study.
Male or female, aged ≥18 years.
Established documented diagnosis of symptomatic HF (NYHA functional class II-III), which has been present for at least 2 months.
LVEF ≤40% documented in the last 3 months by echocardiography or cardiac magnetic resonance.
NT-proBNP ≥600 pg/ml.
Patients should receive background standard of care for HFrEF at judgment of the investigator.
Estimated glomerular filtration rate (eGFR) ≥30 ml/min/1.73m2 (DMRD formula) at enrolment.

Exclusion Criteria:

Inability to perform a valid (respiratory exchange ratio -RER- ≥1.05) baseline cardiopulmonary exercise test (CPET)
Patients receiving therapy with an SGLT2 inhibitor within 8 weeks prior to enrolment, or previous intolerance of an SGLT2 inhibitor
Type 1 diabetes
Symptomatic hypotension or systolic blood pressure <95 mmHg
Current acute decompensated HF or hospitalization due to decompensated HF <4 weeks prior to enrolment
Myocardial infarction, unstable angina, stroke, or transient ischemic attack within 12 weeks prior to enrolment
Coronary revascularization (percutaneous coronary intervention or coronary artery bypass grafting) or cardiac valve repair/replacement within 12 weeks prior to enrolment, or planned to undergo any of these operations after randomization
Implantation of a cardiac resynchronization therapy (CRT) device within 12 weeks prior to enrolment or intent to implant a CRT device
Previous cardiac transplantation or implantation of a ventricular assistance device or similar device, or implantation expected after randomization
HF due to restrictive cardiomyopathy, active myocarditis, constrictive pericarditis, hypertrophic (obstructive) cardiomyopathy, or uncorrected severe primary cardiac valve disease
Symptomatic bradycardia or second or third-degree heart block without a pacemaker
Severe renal dysfunction (eGFR<30 ml/min/1.73m2) or prior admission for acute renal failure in the last 4 weeks.
Pregnant or lactating women
Woman of childbearing age, unless they are using highly effective contraceptive methods.
Patients with severe hepatic impairment (Child-Pugh class C).

Sites / Locations

Hospital Clínico Universitario de Valencia

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Dapagliflozin 10 mg

Placebo identical to dapagliflozin 10 mg

Arm Description

After providing informed consent, patients will be randomly assigned to receive dapagliflozin 10 mg per day.

After providing informed consent, patients will be randomly assigned to receive placebo (one tablet a day orally).

Outcomes

Primary Outcome Measures

Functional capacity

Changes in peak oxygen consumption (VO2) at baseline, 30 and 90 days after starting treatment with dapagliflozin or placebo. VO2 is only one measure and is expressed as milliliters of oxygen per kilogram of body weight per minute (oxygen in milliliters, weight in kilograms, and time in minutes and expressed in ml/kg/min).

Secondary Outcome Measures

Left ventricular volumes

The following parameters will be evaluated: Left ventricular diastolic volume (measured in milliliters, mL) and systolic volume (measured in milliliters, mL) It will be performed by a trained cardiologist blind to study treatment at baseline and at 30 and 90 days after treatment initiation.

Left ventricular ejection fraction

The following parameter will be evaluated: Left ventricular ejection fraction (measured by simpson method and expressed in percentage, %). It will be performed by a trained cardiologist blind to study treatment at baseline and at 30 and 90 days after treatment initiation.

Left atrial volume

The following parameter will be evaluated: Determination of 2-dimensional derived left atrial volume (volumen measured in milliliters, mL) indexed for body surface area (body surface area expressed in square meters -m2-) and expressed in mL/m2. It will be performed by a trained cardiologist blind to study treatment at baseline and at 30 and 90 days after treatment initiation.

Echocardiographic parameters of diastolic function

The following parameter of diastolic function will be evaluated: - E/e' ratio: value of E velocity-expressed in cm/s- / averaged value of septal and lateral side e´velocity - expressed in cm/s- of the mitral annulus by pulsed tissue Doppler. It will be performed by a trained cardiologist blind to study treatment at baseline and at 30 and 90 days after treatment initiation.

Evaluation of health related quality of life by Minnesota Living with Heart Failure Questionnaire (MLHFQ)

Assessment of the quality of life through the Minnesota Living with Heart Failure Questionnaire (MLHFQ). It will be completed at baseline and at 30 and 90 days after treatment initiation. The score values are ranged between 0 to 105 points.

Submáximal functional capacity assesment by 6 minutes walk test

It will be performed in an area equipped for cardiopulmonary resuscitation. Subjects will be asked not to perform vigorous physical exercise in the previous 2 hours. They will be allowed to have a light meal before the test. Before the test, the vital signs will be determined in a seated position after a rest of 10 minutes. Subjects will be instructed to walk at their own pace to cover as much distance (measured in meters) as possible in 6 minutes. It will be performed by a trained nurse blind to study treatment at baseline and at 30 and 90 days after treatment initiation.

Full Information

NCT ID

NCT04197635

First Posted

November 1, 2019

Last Updated

April 21, 2022

Sponsor

Fundación para la Investigación del Hospital Clínico de Valencia

1. Study Identification

Unique Protocol Identification Number

NCT04197635

Brief Title

Short-term Effects of Dapagliflozin on Peak VO2 in HFrEF

Acronym

DAPA-VO2

Official Title

Short-term Effects of Dapagliflozin on Peak VO2 in Patients With Heart Failure With Reduced Ejection Fraction

Study Type

Interventional

2. Study Status

Record Verification Date

April 2022

Overall Recruitment Status

Completed

Study Start Date

June 1, 2019 (Actual)

Primary Completion Date

August 14, 2021 (Actual)

Study Completion Date

April 19, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title

Principal Investigator

Name of the Sponsor

Fundación para la Investigación del Hospital Clínico de Valencia

4. Oversight

Studies a U.S. FDA-regulated Drug Product

Studies a U.S. FDA-regulated Device Product

Data Monitoring Committee

Yes

5. Study Description

Brief Summary

Detailed Description

This study will be a double-blind multicenter randomized study (1:1) to evaluate the effect of dapagliflozin 10 mg per day or placebo on short-term functional capacity evaluated through changes in peak oxygen consumption. This trial will include patients with stable symptomatic heart failure with reduced ejection fraction (HFrEF). Efficacy endpoints will be evaluated at 3 time points: 1) baseline (before dapagliflozin/placebo administration), 2) 30 days after randomization, and, 3) 90 days after randomization. An intermediate clinical visit will be performed one week after study initiation. Pre-and post-treatment evaluations (at baseline, 30 and 90 days) will include clinical assessment, cardiopulmonary exercise stress test, echocardiography, 6-minute walk test (6MWT), and quality of life indicators (Minnesota Living with Heart Failure Questionnaire -MLHFQ). The investigators postulate that dapagliflozin 10 mg/day improves short-term functional capacity of patients with symptomatic HFrEF through multifactorial mechanisms, such as diuretic effect and improvement in myocardial energetic efficiency.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study

Heart Failure With Reduced Ejection Fraction

Keywords

Heart Failure with Reduced Ejection Fraction, Functional Capacity, Quality of life

7. Study Design

Primary Purpose

Treatment

Study Phase

Phase 4

Interventional Study Model

Parallel Assignment

Model Description

This study will be a double-blind multicenter randomized study (1:1) to evaluate the effect of dapagliflozin 10 mg per day or placebo on short-term functional capacity evaluated through changes in peak oxygen consumption The patients will be randomized to receive dapagliflozin or placebo. Once the inclusion criteria are fulfilled and the informed consent signed, patients will be randomized, and efficacy endpoints will be evaluated at 3 time points: 1) baseline (before dapagliflozin/placebo administration), 2) 30 days after randomization, and, 3) 90 days after randomization.

Masking

ParticipantCare ProviderInvestigatorOutcomes Assessor

Masking Description

After providing informed consent, patients will be randomly assigned, with a remote, web-based computer-generated block randomization procedure in an allocation 1:1 ratio, to either receive dapagliflozin 10 mg per day or placebo (one tablet a day orally). This system will allow the maintenance of the randomization codes and the opening of them if necessary. Investigators and patients will be blinded to treatment allocations. Knowing that no treatment crossings between both groups are expected, there is no need of planning washing periods.

Allocation

Randomized

Enrollment

74 (Actual)

8. Arms, Groups, and Interventions

Arm Title

Dapagliflozin 10 mg

Arm Type

Active Comparator

Arm Description

After providing informed consent, patients will be randomly assigned to receive dapagliflozin 10 mg per day.

Arm Title

Placebo identical to dapagliflozin 10 mg

Arm Type

Placebo Comparator

Arm Description

After providing informed consent, patients will be randomly assigned to receive placebo (one tablet a day orally).

Intervention Type

Diagnostic Test

Intervention Name(s)

Maximal functional capacity by cardiopulmonary exercise testing

Other Intervention Name(s)

peak oxygen consumption

Intervention Description

It will be done with cycle ergometer (CORTEX Metamax3B), starting with 10W of power and increasing 10W every minute. During the test, heart rate, rhythm and blood pressure will be monitored. Gas exchange data shall be evaluated every 10 seconds and the peak oxygen consumption (peak VO2) shall be considered the maximum value obtained during the last 20 seconds of exercise. The main parameters to be determined are: maximum functional capacity, peak VO2, slope of the VE/VCO2 ratio, and chronotropic incompetence variables. It will be performed by a trained cardiologist blind to study treatment at baseline and at 30 and 90 days after treatment initiation.

Intervention Type

Diagnostic Test

Intervention Name(s)

Echocardiography

Other Intervention Name(s)

Diastolic and Systolic function

Intervention Description

The following parameters will be evaluated: a)left ventricular volumes; b) left ventricular systolic function; and c)left atrial volume and E/e' ratio. It will be performed by a trained cardiologist blind to study treatment at baseline and at 30 and 90 days after treatment initiation.

Intervention Type

Behavioral

Intervention Name(s)

Evaluation of health related quality of life

Other Intervention Name(s)

Quality of life

Intervention Description

Assessment of the quality of life through the Minnesota Living with Heart Failure Questionnaire (MLHFQ), Spanish version. It will be completed at baseline and at 30 and 90 days after treatment initiation. The score of the questionnaire is 0 to 105 points.

Intervention Type

Diagnostic Test

Intervention Name(s)

Submáximal functional capacity assesment by 6 minutes walk test

Other Intervention Name(s)

6 minutes walk test

Intervention Description

It will be performed in an area equipped for cardiopulmonary resuscitation. Subjects will be asked not to perform a vigorous physical exercise in the previous 2 hours. They will be allowed to have a light meal before the test. Before the test, the vital signs will be determined in a seated position after a rest of 10 minutes. Subjects will be instructed to walk at their own pace to cover as much distance as possible in 6 minutes. It will be performed by a trained nurse blind to study treatment at baseline and at 30 and 90 days after treatment initiation.

Intervention Type

Other

Intervention Name(s)

Clinical evaluation

Intervention Description

Evaluation of signs and symptoms of heart failure

Primary Outcome Measure Information:

Title

Functional capacity

Description

Time Frame