Edwards APTURE Shunt System for Heart Failure

Early Feasibility Study - Edwards APTURE Transcatheter Shunt System

Recruiting N/A Interventional Study
Heart Failure
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
90 (estimated)
Sponsor
Edwards Lifesciences · Industry
Who this trial is looking for

This trial is looking for people with heart failure to evaluate a new device. Participants will need to meet specific health criteria and may need to have recent heart failure events or treatments.

Are You a Good Fit for This Trial?

You may be able to join if

  • I have been diagnosed with heart failure (HFrEF)
  • I experience symptoms classified as NYHA Class II, III, or IVa
  • I have been hospitalized for heart failure in the past year
  • I have had an increase in heart failure treatment recently
  • I have elevated heart failure biomarker levels in the past 6 months
  • I have stable heart failure treatment for at least 6 months

You may not be able to join if

  • I have severe heart failure
  • I have active valve disease
  • I have a body mass index (BMI) of 45 or higher
  • I have had a heart attack or major cardiac procedure in the past 3 months
  • I have had a stroke or similar event in the past 6 months
  • I have renal insufficiency with high creatinine levels
  • I have had a recent infection requiring intravenous antibiotics
  • I have other serious heart function issues

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

Think this trial could be right for you?

Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.

Check Your Eligibility
About This Trial

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

Trial Locations
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Eligibility Criteria
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…
Contacts

Natalie Alon

949-250-1898

Natalie_Alon@edwards.com

CONTACT

Melissa Arteaga

949-250-2002

melissa_arteaga@edwards.com

CONTACT