Tiny heart shunt tested as relief for failing hearts
NCT ID NCT07858799
First seen Oct 05, 2026 · Last updated Oct 06, 2026 · Updated 1 time
Summary
Researchers are testing a device called the Edwards APTURE transcatheter shunt system in people with heart failure and high pressure in the left side of the heart. The shunt is placed through a catheter, without open surgery, to create a new path for blood flow. The study follows 15 participants to check for major heart, brain, or kidney complications and to see whether their heart failure symptoms and quality of life improve over six months.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Edwards APTURE transcatheter shunt system, a device implanted through a catheter to relieve pressure in the heart
- What this could lead to
- If the device works, it could offer a less invasive way to ease heart failure symptoms for people whose left atrial pressure stays high despite medication.
- What could go wrong
- This is a very early, small study of 15 people, so it cannot show whether the device works long term. Implanting a shunt in the heart carries risks of bleeding, infection, or device problems.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
About 15 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
-
Oct 2026
An estimate. Start dates often move.
- Expected to finish
-
Mar 2032
An estimate. End dates often move.
- Lead sponsor
-
A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
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), indicated device therapy, and comorbidity management. 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, or unmet guideline-directed indication for CRT * 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 * Baseline resting heart rate \>100 bpm
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Heart failure are added.
By submitting, you agree to our Terms of use
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The places running it
3 sites. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
-
Herzzentrum Dresden GmbH Universitätsklinik für Innere Medizin und Kardiologie
RECRUITINGDresden, Germany, 01307, Germany
-
Herzzentrum Universitätsklinikum Köln
NOT_YET_RECRUITINGCologne, Germany, 50937, Germany
-
Johannes Gutenberg Universitaet Mainz
RECRUITINGMainz, Germany, 55131, Germany
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Pilot study to determine the optimal protocol for preoperative transcutaneous vagal neurostimulation prior to aortic valve surgery VAGASTIMA - PILOT: a multicenter, randomized study
- The effect of biventricular pacing in heart failure with preserved left ventricular ejection fraction: a pilot mechanistic analysis
- Rural community peer partnerships for improving Methamphetamine-Associated heart failure screening and engagement
- Agreement of the estimated 1-Repetition-Maximum between two Multiple-Repetition-Maximum tests with different weight in patients with cardiovascular disease or risk factors
- Evaluation of the tolerability and safety of the CARDIOMEMS™ intracardiac continuous cardiac hemodynamic monitoring device in patients with cardio renal syndrome with severe renal impairment
- Screening elderly adults in rural communities for heart failure using an NT-proBNP-Guided strategy in china (SEARCH-HF)