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ALT-FLOW II Trial of the Edwards APTURE Transcatheter Shunt System (ALT-FLOW II)

Primary Purpose

Heart Failure

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Edwards APTURE transcatheter shunt system
Sham procedure
Sponsored by
Edwards Lifesciences
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Heart Failure

Eligibility Criteria

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

Key Inclusion Criteria: Symptomatic heart failure A primary diagnosis of HFmrEF or HFpEF (LVEF > 40%), and NYHA class II to ambulatory NYHA class IV (IVa), and Documentation of at least one of the following from the date of initial informed consent: ≥ 1 prior HF hospitalization(s) requiring IV HF therapy in the prior 12 months; AND/OR EITHER BNP value > 35 pg/ml or > 125 pg/ml in permanent or long-term persistent atrial fibrillation; OR NT-proBNP > 125 pg /ml or > 375 pg /ml in permanent or long-term persistent atrial fibrillation There is objective evidence of cardiogenic pulmonary congestion based on hemodynamic criteria obtained by right heart catheterization (RHC) at exercise, and confirmed by hemodynamics core lab as: o Pulmonary capillary wedge pressure at 20 Watts exercise (PCWP 20W) as measured at end-expiration is elevated to ≥ 25 mmHg and PCWP 20W exceeds right atrial pressure (RAP 20W) by ≥ 8 mmHg In the judgment of the treating physician and the Central Screening Committee the patient is on GDMT for HFpEF/HFmrEF for >30 days prior to screening and baseline assessments, that is expected to be maintained without change for 6 months. Key Exclusion Criteria: Severe heart failure defined as one or more of the below: ACC/AHA/ESC Stage D HF, non-ambulatory NYHA Class IV HF If Body Mass Index (BMI) < 30, cardiac index < 2.0 L/min/m2 If BMI ≥ 30, cardiac index < 1.8 L/min/m2 Inotropic infusion (continuous or intermittent) within the past 6 months Patient is on the cardiac transplant waiting list Prior diagnosis of HF with reduced ejection fraction (HFrEF), including patients with improvement in LVEF to > 40% Valve disease: Degenerative mitral regurgitation > moderate Functional or secondary mitral valve regurgitation defined as grade > moderate Mitral stenosis > mild Primary or secondary tricuspid valve regurgitation defined as grade > moderate Aortic valve disease defined as aortic regurgitation grade > moderate or aortic stenosis > moderate More than mild right ventricular (RV) dysfunction as determined by the echo core lab, taking into account the following available parameters: Tricuspid annular plane systolic excursion (TAPSE) <1.4 cm, or RV size ≥ LV size Right ventricular ejection fraction (RVEF) < 35%; OR Imaging or clinical evidence of congestive hepatopathy Mean right atrial pressure (mRAP) > 15 mmHg at rest Pulmonary vascular resistance (PVR) ≥ 5.0 WU BMI ≥ 45 Myocardial infarction (MI) and/or any therapeutic invasive, non-valvular cardiovascular procedure within past 3 months or current indication for coronary revascularization Stroke, transient ischemic attack (TIA), deep vein thrombosis (DVT) or pulmonary embolus within the past 6 months Renal insufficiency as determined by creatinine (sCr) level > 2.5 mg/dL or estimated glomerular filtration rate (eGFR) < 25ml/min/1.73 m2 by CKD-Epi equation; or currently requiring dialysis Performance of the six-minute walk test (6MWT) with a distance < 50m OR > 450m Active endocarditis or infection requiring intravenous antibiotics within 3 months

Sites / Locations

  • The Ohio State UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

APTURE shunt + medical therapy

Sham + medical therapy

Arm Description

Outcomes

Primary Outcome Measures

Device + Medical Therapy: Subjects with Early Major Adverse Events
Shunt implant safety: proportion of patients in the APTURE shunt group without any serious device or procedure-related (CEC adjudicated) complications (i.e., Major Adverse Cardiovascular, Cerebrovascular, and Renal Events [MACCRE]; at 30 days post index procedure or hospital discharge, whichever is later.
Mean change in PCWP from baseline at 20W exercise
Hemodynamic Effectiveness: change in PCWP at 20W exercise from baseline (mmHg) at 6 months.

Secondary Outcome Measures

KCCQ-OSS change from baseline at 6-month follow-up
Proportion of individual patient success defined as being free from death, disabling stroke, and HF hospitalization with at least (≥) a 15-point improvement from baseline KCCQ-OSS or at least (≥) a 25m improvement from baseline 6MWT.
6MWT change from baseline at 6-month follow-up

Full Information

First Posted
January 6, 2023
Last Updated
September 5, 2023
Sponsor
Edwards Lifesciences
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1. Study Identification

Unique Protocol Identification Number
NCT05686317
Brief Title
ALT-FLOW II Trial of the Edwards APTURE Transcatheter Shunt System
Acronym
ALT-FLOW II
Official Title
A Randomized, Sham-controlled Clinical Trial for Evaluation of the Edwards APTURE Transcatheter Shunt System (ALT-FLOW II)
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
April 1, 2023 (Actual)
Primary Completion Date
October 31, 2024 (Anticipated)
Study Completion Date
October 31, 2029 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Edwards Lifesciences

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Device Product Not Approved or Cleared by U.S. FDA
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This is a prospective, multi-center, randomized, sham-controlled clinical trial.
Detailed Description
The objectives of this trial are to assess the safety, performance, and effectiveness of the Edwards APTURE transcatheter shunt system when used for the treatment of patients with heart failure with preserved (HFpEF) or mildly reduced (HFmrEF) ejection fraction (LVEF >40%) who remain symptomatic despite guideline-directed medical therapy (GDMT)

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
APTURE shunt + medical therapy
Arm Type
Experimental
Arm Title
Sham + medical therapy
Arm Type
Sham Comparator
Intervention Type
Device
Intervention Name(s)
Edwards APTURE transcatheter shunt system
Intervention Description
Treatment with APTURE shunt
Intervention Type
Diagnostic Test
Intervention Name(s)
Sham procedure
Intervention Description
CS angiography
Primary Outcome Measure Information:
Title
Device + Medical Therapy: Subjects with Early Major Adverse Events
Description
Shunt implant safety: proportion of patients in the APTURE shunt group without any serious device or procedure-related (CEC adjudicated) complications (i.e., Major Adverse Cardiovascular, Cerebrovascular, and Renal Events [MACCRE]; at 30 days post index procedure or hospital discharge, whichever is later.
Time Frame
30 days
Title
Mean change in PCWP from baseline at 20W exercise
Description
Hemodynamic Effectiveness: change in PCWP at 20W exercise from baseline (mmHg) at 6 months.
Time Frame
6-months
Secondary Outcome Measure Information:
Title
KCCQ-OSS change from baseline at 6-month follow-up
Time Frame
6-months
Title
Proportion of individual patient success defined as being free from death, disabling stroke, and HF hospitalization with at least (≥) a 15-point improvement from baseline KCCQ-OSS or at least (≥) a 25m improvement from baseline 6MWT.
Time Frame
6-months
Title
6MWT change from baseline at 6-month follow-up
Time Frame
6-months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Key Inclusion Criteria: Symptomatic heart failure A primary diagnosis of HFmrEF or HFpEF (LVEF > 40%), and NYHA class II to ambulatory NYHA class IV (IVa), and Documentation of at least one of the following from the date of initial informed consent: ≥ 1 prior HF hospitalization(s) requiring IV HF therapy in the prior 12 months; AND/OR EITHER BNP value > 35 pg/ml or > 125 pg/ml in permanent or long-term persistent atrial fibrillation; OR NT-proBNP > 125 pg /ml or > 375 pg /ml in permanent or long-term persistent atrial fibrillation There is objective evidence of cardiogenic pulmonary congestion based on hemodynamic criteria obtained by right heart catheterization (RHC) at exercise, and confirmed by hemodynamics core lab as: o Pulmonary capillary wedge pressure at 20 Watts exercise (PCWP 20W) as measured at end-expiration is elevated to ≥ 25 mmHg and PCWP 20W exceeds right atrial pressure (RAP 20W) by ≥ 8 mmHg In the judgment of the treating physician and the Central Screening Committee the patient is on GDMT for HFpEF/HFmrEF for >30 days prior to screening and baseline assessments, that is expected to be maintained without change for 6 months. Key Exclusion Criteria: Severe heart failure defined as one or more of the below: ACC/AHA/ESC Stage D HF, non-ambulatory NYHA Class IV HF If Body Mass Index (BMI) < 30, cardiac index < 2.0 L/min/m2 If BMI ≥ 30, cardiac index < 1.8 L/min/m2 Inotropic infusion (continuous or intermittent) within the past 6 months Patient is on the cardiac transplant waiting list Prior diagnosis of HF with reduced ejection fraction (HFrEF), including patients with improvement in LVEF to > 40% Valve disease: Degenerative mitral regurgitation > moderate Functional or secondary mitral valve regurgitation defined as grade > moderate Mitral stenosis > mild Primary or secondary tricuspid valve regurgitation defined as grade > moderate Aortic valve disease defined as aortic regurgitation grade > moderate or aortic stenosis > moderate More than mild right ventricular (RV) dysfunction as determined by the echo core lab, taking into account the following available parameters: Tricuspid annular plane systolic excursion (TAPSE) <1.4 cm, or RV size ≥ LV size Right ventricular ejection fraction (RVEF) < 35%; OR Imaging or clinical evidence of congestive hepatopathy Mean right atrial pressure (mRAP) > 15 mmHg at rest Pulmonary vascular resistance (PVR) ≥ 5.0 WU BMI ≥ 45 Myocardial infarction (MI) and/or any therapeutic invasive, non-valvular cardiovascular procedure within past 3 months or current indication for coronary revascularization Stroke, transient ischemic attack (TIA), deep vein thrombosis (DVT) or pulmonary embolus within the past 6 months Renal insufficiency as determined by creatinine (sCr) level > 2.5 mg/dL or estimated glomerular filtration rate (eGFR) < 25ml/min/1.73 m2 by CKD-Epi equation; or currently requiring dialysis Performance of the six-minute walk test (6MWT) with a distance < 50m OR > 450m Active endocarditis or infection requiring intravenous antibiotics within 3 months
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Bridget Hurley
Phone
(949) 250-2265
Email
bridget_hurley@edwards.com
First Name & Middle Initial & Last Name or Official Title & Degree
Melissa Arteaga
Phone
(949) 250-2002
Email
melissa_arteaga@edwards.com
Facility Information:
Facility Name
The Ohio State University
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43210
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Maeve McLoughlin, MPH
Phone
614-292-4084
Email
maeve.mcloughlin@osumc.edu
First Name & Middle Initial & Last Name & Degree
Annie Kellum
Phone
614-366-8848
Email
annie.kellum@osumc.edu
First Name & Middle Initial & Last Name & Degree
Scott Lilly, MD
First Name & Middle Initial & Last Name & Degree
Rami Kahwash, MD

12. IPD Sharing Statement

Learn more about this trial

ALT-FLOW II Trial of the Edwards APTURE Transcatheter Shunt System

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