WebASCEND-HF was a randomized trial of nesiritide vs. placebo in 7141 patients hospitalized with acute HF in which dyspnoea relief at 6 h was measured on a 7-point Likert scale. Patients were classified as having early dyspnoea relief if they experienced moderate or marked dyspnoea improvement at 6 h. WebMar 18, 2024 · Title: RELIEVE-HF TRIAL: REducing Lung congestIon symptoms using the V-wavE shunt in adVancEd Heart Failure. PI: Zvonimir Krajcer, MD Sponsor: V-Wave, Ltd. NCT03499236. Eligibility Requirements. Heart failure with reduced ejection fraction (HFrEF) and heart failure with preserved ejection fraction (HFpEF) patients
Novel Interatrial Shunt Shows Promise at 1 Year in HF Patients …
WebOct 25, 2024 · In the trial, the roll-in arm patients received treatment with the Ventura device. No device- or procedure-related major adverse cardiac or neurological events have been reported so far. V-Wave chief medical officer Dr William Abraham said: “RELIEVE-HF is the gold standard in being the most comprehensive trial of interatrial shunting in HF to ... WebNov 5, 2024 · Forxiga is currently being tested for patients with HF in the DELIVER (HF with preserved ejection fraction, HFpEF) and DETERMINE (HFrEF and HFpEF) Phase III trials. Forxiga will also be tested in patients without T2D following an acute myocardial infarction (MI) or heart attack in the DAPA-MI trial - a first of its kind, indication-seeking, registry … dim the rhino beetle
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WebApr 17, 2024 · Masking Description: In the randomized cohort, participants, the clinical team, and research staff managing the patient after randomization will be blinded to study assignment. Primary Purpose: Treatment. Official Title: RELIEVE-HF TRIAL: REducing Lung congestIon Symptoms Using the v-wavE Shunt in adVancEd Heart Failure. WebFeb 2, 2024 · The randomized RELIEVE-HF trial is testing the Ventura Interatrial Shunt (V-Wave) in patients with symptomatic HF across the full spectrum of ejection fraction, from reduced (HFrEF) to HFpEF. The study is still underway at 120 sites internationally but today, during a late-breaking session at the Technology and Heart Failure Therapeutics (THT ... WebBackground: A randomized, sham-controlled trial in patients with heart failure (HF) and left ventricular ejection fraction (LVEF) ≥40% demonstrated reductions in pulmonary capillary wedge pressure (PCWP) with a novel transcatheter InterAtrial Shunt Device (IASD). Whether this hemodynamic effect will translate to an improvement in cardiovascular outcomes … fortitude valley to brisbane