Recruiting

Edwards APTURE

Sponsor:

Edwards Lifesciences

Code:

NCT03523416

Conditions

Heart Failure

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

Edwards APTURE transcatheter shunt system

Study Details

Brief summary:

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

Conditions

Heart Failure

Study ID

NCT03523416

Start date

Jul 31, 2018

Status verified date

Sep, 2026

Completion date

Apr, 2032

Anticipated

Primary completion date

Apr, 2027

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

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:

1. Mean pulmonary capillary wedge pressure (PCWP) >35 mmHg
2. Mean right atrial pressure (RAP) >15 mmHg
3. Mean PCWP-mean RAP gradient < 5 mmHg
4. Pulmonary vascular resistance (PVR) ≥5 Wood Units (WU)
5. Cardiac index <1.8 L/min/m2

Study Design

Enrollment

90 participants

Anticipated

Intervention Model

Single group

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Edwards APTURE transcatheter shunt system

Interventions

Edwards APTURE transcatheter shunt system

Transcatheter treatment of symptomatic heart failure patients with elevated left atrial pressure.

Primary outcome measure

  • Rate of major cardiac/cerebrovascular/renal events and re-intervention (Safety Endpoint) [ Time Frame: 30 days ]

Central Contacts and Locations

Locations

The Ohio State University Medical Center

Recruiting

Columbus, Ohio, United States, 43210

Contacts

Principal Investigator:

Scott Lilly, MD

Oklahoma Heart Institute

Recruiting

Tulsa, Oklahoma, United States, 74104

Contacts

Principal Investigator:

Kamran Muhammad, MD

More Information

Sponsor

Edwards Lifesciences

Last update posted

Oct 2, 2026

Last verified

Sep, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-10-03. This information was provided to ClinicalTrials.gov by Edwards Lifesciences on 2026-10-02. Recruitment status is synced daily from ClinicalTrials.gov and may not reflect the sponsor's current status. Confirm during your call.