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NCT03523416Recruiting

Early Feasibility Study - Edwards APTURE Transcatheter Shunt System

Early Feasibility Study of the Edwards APTURE Transcatheter Shunt System (ALT-FLOW US)

Source: ClinicalTrials.gov · Last updated 2 Oct 2026

Brief summary (registry, in English)

The purpose of this study is to evaluate initial clinical safety, device functionality and effectiveness of the Edwards APTURE transcatheter shunt system.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
90 (estimated)
First submitted
12 Apr 2018
Start date
31 Jul 2018
Primary completion date
Apr 2027
Lead sponsor
Edwards Lifesciences
NCT number
NCT03523416

What you commit to

  • Study type: Interventional
  • Planned participants: 90
  • From 31 Jul 2018 to the primary completion date, Apr 2027
  • 19 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Criteria the registry did not label

  • Refined HFrEF Subgroup Inclusion Criteria:
  • A primary diagnosis of HFrEF (LVEF ≤ 40%), and
  • NYHA Class II, III, or IVa heart failure symptoms and
  • Documentation of at least one of the following in the past 12 months, such as:
    • Hospitalization for heart failure; or
    • Increased treatment for heart failure, including intravenous (IV) or higher-dose diuretic therapy.
    • Elevated heart failure biomarker levels (BNP or NT-proBNP) within the past 6 months.
    • Note: Participants with NYHA Class II symptoms must have both a recent heart failure worsening event and elevated biomarker levels. Participants with NYHA Class III or IVa symptoms must have either a recent heart failure worsening event or elevated biomarker levels.
  • Stable Optimized GDMT - Maintained 6 months post-implant (includes stable GLP-1 RA)
    • Refined HFrEF Subgroup Exclusion Criteria:
  • Severe HF defined as one or more of the following:
    • Ambulatory NT-proBNP value \>5,000 pg/ml or BNP value \>1,600 pg/ml
    • Left ventricular end-diastolic diameter (LVEDD) \>8 cm
    • Left ventricular ejection fraction (LVEF) \< 20%
    • ACC/AHA Stage D HF or non-ambulatory NYHA Class IV HF
    • Inotropic infusion (continuous or intermittent) within the past 6 months
    • Active listing on the cardiac transplant waiting list
  • More than mild right ventricular dysfunction
  • Valve disease
    • Mitral regurgitation \> moderate
    • Mitral stenosis \> mild
    • Tricuspid regurgitation \> moderate
    • Aortic regurgitation \> moderate
    • Aortic stenosis \> moderate
  • Body mass index (BMI) ≥45
  • Myocardial infarction and/or any therapeutic invasive, non-valvular cardiac procedure within the past 3 months, or current indication for coronary revascularization
  • Stroke, transient ischemic attack, deep vein thrombosis, or pulmonary embolus within the past 6 months
  • Cardiac resynchronization therapy implanted within the past 12 months
  • Renal insufficiency as determined by serum creatinine (sCr) level \>2.5 mg/dL or estimated glomerular filtration rate (eGFR) \<25 ml/min/1.73 m2
  • Performance of the 6-minute walk test with a distance \<100 m or \>450 m
  • Active endocarditis or infection requiring intravenous antibiotics within 3 months of scheduled index procedure
  • Presence of one or more of the following resting hemodynamic findings:
    • Mean pulmonary capillary wedge pressure (PCWP) \>35 mmHg
    • Mean right atrial pressure (RAP) \>15 mmHg
    • Mean PCWP-mean RAP gradient \< 5 mmHg
    • Pulmonary vascular resistance (PVR) ≥5 Wood Units (WU)
    • Cardiac index \<1.8 L/min/m2

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (19)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Colorado
Coordinator of this site? Confirm its status
AuroraUnited StatesWithdrawn
Medical University of South Carolina
Coordinator of this site? Confirm its status
CharlestonUnited StatesActive, not recruiting
Atrium Health
Coordinator of this site? Confirm its status
CharlotteUnited StatesCompleted
The Christ Hospital
Coordinator of this site? Confirm its status
CincinnatiUnited StatesActive, not recruiting
The Ohio State University Medical Center
Coordinator of this site? Confirm its status
ColumbusUnited StatesRecruiting
St. Vincent Medical Group
Coordinator of this site? Confirm its status
IndianapolisUnited StatesCompleted
University of Florida Health Jacksonville
Coordinator of this site? Confirm its status
JacksonvilleUnited StatesActive, not recruiting
Kansas University Medical Center
Coordinator of this site? Confirm its status
Kansas CityUnited StatesActive, not recruiting
UC San Diego Health
Coordinator of this site? Confirm its status
La JollaUnited StatesActive, not recruiting
Cedars-Sinai Medical Center
Coordinator of this site? Confirm its status
Los AngelesUnited StatesWithdrawn
Abbott Northwestern
Coordinator of this site? Confirm its status
MinneapolisUnited StatesActive, not recruiting
Morristown Medical Center
Coordinator of this site? Confirm its status
MorristownUnited StatesWithdrawn
Oregon Health and Science University
Coordinator of this site? Confirm its status
PortlandUnited StatesActive, not recruiting
Mayo Clinic
Coordinator of this site? Confirm its status
RochesterUnited StatesActive, not recruiting
University California San Francisco
Coordinator of this site? Confirm its status
San FranciscoUnited StatesActive, not recruiting
Swedish Medical Center
Coordinator of this site? Confirm its status
SeattleUnited StatesActive, not recruiting
Montefiore Medical Center
Coordinator of this site? Confirm its status
The BronxUnited StatesActive, not recruiting
Oklahoma Heart Institute
Coordinator of this site? Confirm its status
TulsaUnited StatesRecruiting
Lankenau Institute for Medical Research
Coordinator of this site? Confirm its status
WynnewoodUnited StatesCompleted

This page is information, not medical advice. Discuss any trial with your doctor.