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
- Diseases
- Heart failure
- 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
Sites (19)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| University of Colorado Coordinator of this site? Confirm its status | Aurora | United States | Withdrawn |
| Medical University of South Carolina Coordinator of this site? Confirm its status | Charleston | United States | Active, not recruiting |
| Atrium Health Coordinator of this site? Confirm its status | Charlotte | United States | Completed |
| The Christ Hospital Coordinator of this site? Confirm its status | Cincinnati | United States | Active, not recruiting |
| The Ohio State University Medical Center Coordinator of this site? Confirm its status | Columbus | United States | Recruiting |
| St. Vincent Medical Group Coordinator of this site? Confirm its status | Indianapolis | United States | Completed |
| University of Florida Health Jacksonville Coordinator of this site? Confirm its status | Jacksonville | United States | Active, not recruiting |
| Kansas University Medical Center Coordinator of this site? Confirm its status | Kansas City | United States | Active, not recruiting |
| UC San Diego Health Coordinator of this site? Confirm its status | La Jolla | United States | Active, not recruiting |
| Cedars-Sinai Medical Center Coordinator of this site? Confirm its status | Los Angeles | United States | Withdrawn |
| Abbott Northwestern Coordinator of this site? Confirm its status | Minneapolis | United States | Active, not recruiting |
| Morristown Medical Center Coordinator of this site? Confirm its status | Morristown | United States | Withdrawn |
| Oregon Health and Science University Coordinator of this site? Confirm its status | Portland | United States | Active, not recruiting |
| Mayo Clinic Coordinator of this site? Confirm its status | Rochester | United States | Active, not recruiting |
| University California San Francisco Coordinator of this site? Confirm its status | San Francisco | United States | Active, not recruiting |
| Swedish Medical Center Coordinator of this site? Confirm its status | Seattle | United States | Active, not recruiting |
| Montefiore Medical Center Coordinator of this site? Confirm its status | The Bronx | United States | Active, not recruiting |
| Oklahoma Heart Institute Coordinator of this site? Confirm its status | Tulsa | United States | Recruiting |
| Lankenau Institute for Medical Research Coordinator of this site? Confirm its status | Wynnewood | United States | Completed |
This page is information, not medical advice. Discuss any trial with your doctor.