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Hemodynamic Response to Exercise in HFpEF Patients After Upregulation of SERCA2a

Primary Purpose

Heart Failure, Congestive

Status
Completed
Phase
Early Phase 1
Locations
United States
Study Type
Interventional
Intervention
Istaroxime
Exercise
Sponsored by
Benjamin Levine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Heart Failure, Congestive

Eligibility Criteria

60 Years - 85 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Healthy Senior Controls

Inclusion Criteria:

  • age > 60 years

Exclusion Criteria:

  • Coronary Ischemia
  • No chronic medical problems
  • BMI > 30 kg/m2

HFpEF Subjects

Inclusion Criteria:

  • age > 60 years
  • signs and symptoms of heart failure
  • ejection fraction > 50%
  • objective evidence of diastolic dysfunction

Exclusion Criteria:

  • Coronary Ischemia
  • Chronic Kidney Disease, stage 4 or greater
  • Persistent atrial fibrillation
  • Severe valvular disease
  • BMI > 45 kg/m2

Sites / Locations

  • The Institute for Exercise and Environmental Medicine

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Healthy Senior Control

Heart failure patients

Arm Description

Fifteen healthy senior subjects will perform light exercise at a fixed heart rate of 100 beats per minute. Subjects will then be given either placebo infusion (normal saline) or Istaroxime infusion for one hour. Subjects will be blinded to which infusion they are receiving. Subjects will then repeat light exercise at a fixed heart rate of 100 beats per minute. Primary outcome is changes in cardiac filling pressures during exercise.

Fifteen HFpEF subjects will perform light exercise at a fixed heart rate of 100 beats per minute. Subjects will then be given either placebo infusion (normal saline) or Istaroxime infusion for one hour. Subjects will be blinded to which infusion they are receiving. Subjects will then repeat light exercise at a fixed heart rate of 100 beats per minute. Primary outcome is changes in cardiac filling pressures during exercise.

Outcomes

Primary Outcome Measures

Change in cardiac filling pressures (pulmonary capillary wedge pressure) during exercise with Istaroxime
Change in cardiac filling pressures (pulmonary capillary wedge pressure) during exercise with Istaroxime

Secondary Outcome Measures

Change in cardiac relaxation time (isovolumic relaxation time) during exercise with Istaroxime
Change in cardiac relaxation time (isovolumic relaxation time) during exercise

Full Information

First Posted
May 11, 2016
Last Updated
June 22, 2022
Sponsor
Benjamin Levine
Collaborators
National Institute on Aging (NIA)
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1. Study Identification

Unique Protocol Identification Number
NCT02772068
Brief Title
Hemodynamic Response to Exercise in HFpEF Patients After Upregulation of SERCA2a
Official Title
Hemodynamic Response to Exercise in Heart Failure With Preserved Ejection Fraction (HFpEF) Patients After Upregulation of SERCA2a
Study Type
Interventional

2. Study Status

Record Verification Date
June 2022
Overall Recruitment Status
Completed
Study Start Date
September 15, 2015 (Actual)
Primary Completion Date
December 1, 2018 (Actual)
Study Completion Date
December 1, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Benjamin Levine
Collaborators
National Institute on Aging (NIA)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Heart failure with preserved ejection fraction or HFpEF, represents nearly 50% of all heart failure cases and is particularly common in the elderly. The disease has no current treatment options. Symptoms typically occur during exertion or exercise and is likely the result of increased cardiac and pulmonary congestion as a result of impaired diastolic function. Istaroxime is a novel activator of SERCA2a, an important regulator of calcium uptake within the myocyte. We will test the hypothesis that Istaroxime will improve diastolic function during exercise in HFpEF patients which in turn will reduce cardiac and pulmonary congestion.
Detailed Description
About half of all elderly patients with a diagnosis of congestive heart failure have apparently normal systolic function, so called "heart failure with a preserved ejection fraction" or HFpEF. To date, no effective therapy for HFpEF has been found, in part because of failure to discern key pathophysiologic pathways. An extensive amount of pre-clinical work has identified that altered sarcoplasmic reticulum (SR) Ca2+ uptake, storage, and release play a major role in the changes in cardiac relaxation associated with aging, especially regarding sequestration of Ca++ by the sarcoplasmic reticular Ca++-ATPase (SERCA2a), which causes cardiac muscle relaxation by reducing cytosolic Ca++. Istaroxime is a relatively new drug that augments lusitropic function by upregulating SERCA2a activity in the heart. Because of the clear importance of slowed relaxation in HFpEF, and the evidence that depressed SERCA2a activity contributes to the slowed relaxation with aging, the proposed study may be establish the "impairment of SERCA2a" hypothesis as a mechanism of impaired relaxation in HFpEF subjects.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Basic Science
Study Phase
Early Phase 1
Interventional Study Model
Parallel Assignment
Model Description
Two separate groups of subjects (senior controls and patients with HFpEF) receiving istaroxime
Masking
Participant
Allocation
Non-Randomized
Enrollment
26 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Healthy Senior Control
Arm Type
Active Comparator
Arm Description
Fifteen healthy senior subjects will perform light exercise at a fixed heart rate of 100 beats per minute. Subjects will then be given either placebo infusion (normal saline) or Istaroxime infusion for one hour. Subjects will be blinded to which infusion they are receiving. Subjects will then repeat light exercise at a fixed heart rate of 100 beats per minute. Primary outcome is changes in cardiac filling pressures during exercise.
Arm Title
Heart failure patients
Arm Type
Experimental
Arm Description
Fifteen HFpEF subjects will perform light exercise at a fixed heart rate of 100 beats per minute. Subjects will then be given either placebo infusion (normal saline) or Istaroxime infusion for one hour. Subjects will be blinded to which infusion they are receiving. Subjects will then repeat light exercise at a fixed heart rate of 100 beats per minute. Primary outcome is changes in cardiac filling pressures during exercise.
Intervention Type
Drug
Intervention Name(s)
Istaroxime
Other Intervention Name(s)
exercise
Intervention Description
Subjects will be given Istaroxime, a novel SERCA2a activator one hour prior and during exercise.
Intervention Type
Other
Intervention Name(s)
Exercise
Primary Outcome Measure Information:
Title
Change in cardiac filling pressures (pulmonary capillary wedge pressure) during exercise with Istaroxime
Description
Change in cardiac filling pressures (pulmonary capillary wedge pressure) during exercise with Istaroxime
Time Frame
Immediate; 90 minutes after infusion
Secondary Outcome Measure Information:
Title
Change in cardiac relaxation time (isovolumic relaxation time) during exercise with Istaroxime
Description
Change in cardiac relaxation time (isovolumic relaxation time) during exercise
Time Frame
90 minutes

10. Eligibility

Sex
All
Minimum Age & Unit of Time
60 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Healthy Senior Controls Inclusion Criteria: age > 60 years Exclusion Criteria: Coronary Ischemia No chronic medical problems BMI > 30 kg/m2 HFpEF Subjects Inclusion Criteria: age > 60 years signs and symptoms of heart failure ejection fraction > 50% objective evidence of diastolic dysfunction Exclusion Criteria: Coronary Ischemia Chronic Kidney Disease, stage 4 or greater Persistent atrial fibrillation Severe valvular disease BMI > 45 kg/m2
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Benjamin D Levine, MD
Organizational Affiliation
UT Southwestern
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Institute for Exercise and Environmental Medicine
City
Dallas
State/Province
Texas
ZIP/Postal Code
75231
Country
United States

12. IPD Sharing Statement

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Hemodynamic Response to Exercise in HFpEF Patients After Upregulation of SERCA2a

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