NCT05677100ClinicalTrials.gov

Diuretics Alone vs. Aortix Endovascular Device for Acute Heart Failure

DRAIN-HF: Diuretics Alone vs. Aortix Endovascular Device for Acute Heart Failure

In reclutamentoAccetta partecipanti ora, secondo la scheda del registro.

Contatta questo studio

In breve

Aortix is a circulatory support device for chronic heart failure patients on medical management who have been hospitalized for acute decompensated heart failure (ADHF) and have persistent congestion despite usual medical therapy. Eligible ADHF patients with diuretic resistance (irrespective of…

Interventistico320 partecipanti ricercati50 centri2 paesi

Categorie

Cardiovascolare84%Nefrologia e urologia13%Ostetricia e ginecologia3%

Registrato in 1 registro

ClinicalTrials.govNCT05677100Apri questa scheda su ClinicalTrials.govSincronizzato 4 settimane fa

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How this study is set up

The points below are drawn from the public registry record for this study. Each one cites the field or sentence it came from. A dash (—) means the record does not state something — not that it is missing or wrong. Many well-run studies, especially small ones, leave some of these blank.

Present: Registered before enrolment beganFirst posted 2023-01-10; recorded start 2023-08-23
Present: Has a defined primary outcomeA primary outcome measure is listed in the record
Present: The primary outcome states a time frameThe primary outcome measure records a time frame
Present: Participants are randomly assignedAllocation is recorded as randomised
Present: Has a comparison groupThe record lists a placebo or comparator arm, or more than one study arm
Not stated: Open label (no blinding)Masking is recorded as none (open label)
Not stated: An ethics committee is not stated in the registry recordThis registry's ingested record has no ethics-committee field
Not stated: Regulatory oversight (such as an IND or IDE) is not stated in the registry recordThis registry's ingested record has no regulatory-authorisation field
Not stated: A data monitoring committee is not stated in the registry recordThis registry's ingested record has no data-monitoring-committee fieldA data monitoring committee is not required for many smaller studies, and its absence here is not unusual.
Present: No cost to participants is mentioned in the recordChecked the summary, description and eligibility text; no cost-to-participant phrase found
Not stated: No other studies from this sponsor are in this databaseCounted from the lead sponsor named in the record (Procyrion)
Not stated: No posted results from this sponsor are in this database yetBased on the sponsor’s studies in this database

The record lists 8 conditions.
Lead sponsor type recorded as: industry.

These are facts from the public registry record, not a judgement about the study. Discuss any trial with your own doctor before taking part.

What these facts mean, and what to ask · ruleset v1

Trial stature

Three independent measures of this study, described from its registry record — not a recommendation about it. A rigorous study by investigators nobody has heard of is better evidence than a weak study led by a famous one. How these are scored.

Methodological rigourMODERATE

A moderately rigorous design for a study of this type, judged from its ClinicalTrials.gov record.

How this score is built

Randomised allocation20/20
Participants are randomly allocated between arms
Blinding0/20
Open-label
Control arm0/15
No comparator arm stated in the record
Primary-outcome specificity10/10
Named primary outcome with a defined time frame
Endpoint type3/10
Surrogate or intermediate endpoint (conservative default)
Multi-centre8/8
Multi-centre: 49 sites
Data monitoring committee7/7
A data monitoring committee is in place
Prospective registration5/5
Registered before the study start date
Protocol / SAP posted0/5
No protocol or SAP posted to the registry

ScaleMEDIUM

A medium-sized study, international in scope: 320 participants (target), run at 50 sites, across 2 countries.

How this score is built

Enrolment24/40
320 participants (target)
Site count20/25
49 sites
Country count7/15
2 countries
Planned duration9/10
Planned over about 48 months
Sponsor scale0/10
Procyrion has led 1 trials in our corpus

Investigator standingUNKNOWN

We have no verifiable track record for the investigator named on this trial. That is common for early-career investigators and for records held outside ClinicalTrials.gov — it is not a negative signal.

How this score is built

Investigator standing0/100
No investigator recorded in the registry for this trial

These describe the registry record only, and today we hold ClinicalTrials.gov data. Absent fields lower a score, and absence often reflects registration practice rather than study quality. A high-stature trial is not necessarily safer or a better choice for you — enrolling in a large definitive trial can mean a higher chance of receiving placebo, while a small early-phase study may be the only route to a new therapy.

Sintesi

The study is a prospective, multi-center, randomized, nonblinded study to evaluate the safety and effectiveness of the Aortix System versus standard of care medical therapy in patients hospitalized with acute decompensated heart failure (ADHF) and persistent congestion despite usual medical management.Eligible ADHF patients with diuretic resistance (irrespective of ejection fraction) will be enrolled and randomized 1:1 to either the Aortix system or standard of care medical management. Randomization will be stratified by ejection fraction.. An additional registry arm will enroll patients who are considered candidates for advanced therapies in the near-term, but need improvement in their renal function to be able to receive additional medical therapies. All eligible enrolled registry subjects will receive Aortix system support. Planned study population is male or female patients 21 years of age or greater, with acute decompensated heart failure and diuretic resistance who remain congested despite standard of care medical therapy. This study will enroll up to 320 subjects with heart failure at 50 clinical sites in the United States and up to 5 OUS sites. The randomized study includes up to 240 subjects and the Advanced HF registry includes up to 80 subjects.

Patologie

Heart Failure
Cardiorenal Syndrome
Cardio-Renal Syndrome
ADHF
Heart Failure, Systolic
Heart Failure, Diastolic
Heart Failure; With Decompensation
Heart Failure, Congestive

Idoneità

Idoneità
Sesso	Tutti
Età	21 Years – Nessun massimo
Volontari sani	No

Idoneità come riportata nel registro

Inclusion Criteria (Randomized Study): * Currently admitted to the hospital with a primary diagnosis of decompensated heart failure, irrespective of ejection fraction (EF); * Patients should be on maximally tolerated diuretic therapy and not diuresing sufficiently before being enrolled in DRAIN-HF. After being up-titrated on diuretics, patients should be followed for at least 24 hours on the higher of: i) furosemide 80 mg IV bid or equivalent or ii) IV furosemide or equivalent IV loop diuretic at a dose 2.5 x total daily home dose of furosemide equivalents in 2 divided doses, as tolerated, patient must have: Urine Output \<1,500mL in a 12-hour period OR a Net Fluid Loss ≤375mL in a 12-hour period. * Persistent signs and/or symptoms of congestion as evidenced by at least 2+ pitting edema, elevated jugular venous pressure \>12 cm water or ascites after treatment with IV diuretics per inclusion criterion 2.; * Age \>21 years and able to provide written informed consent; * Negative pregnancy test if patient is of child-bearing potential. Exclusion Criteria (Randomized Study): * Treatment with high dose IV inotropes within the last 48 hours prior to enrollment. High dose is defined as \>5 µg/kg/min dopamine OR \>5 µg/kg/min dobutamine OR \>0.375 µg/kg/min milrinone; * Active and ongoing hypotension with a systolic blood pressure \<90 mmHg lasting more than 30 minutes or a mean arterial pressure (MAP) \<60 mmHg lasting more than 30 minutes at enrollment; * Treatment with vasopressors (defined as phenylephrine, norepinephrine, epinephrine or, vasopressin) within 48 hours prior to enrollment; * An estimated PASP of \>80 mmHg as measured on echocardiogram or echocardiographic evidence of primarily right heart failure; * Acute kidney failure defined as an increase in serum creatinine to ≥4.0mg/dL (≥353.6 µmol/L) at enrollment; * Evidence of contrast induced nephropathy, nephritis or nephrotic syndrome; * Prior kidney transplant, single kidney, partial nephrectomy OR use of dialysis, continuous renal replacement therapy (CRRT) or ultrafiltration in the last 90 days prior to enrollment; * Confirmed decompensated cirrhosis (defined as Child Pugh class B or C) or concern for shock liver (AST \> 1000U/L or total Bilirubin \> 5.0mg/dl) at enrollment; * Presence of an active, uncontrolled infection that would preclude safe placement or removal of the device; * Prior heart transplant or likely heart transplantation before the 30- day follow-up visit; * Current or previous support with a durable LVAD at any time or planned LVAD insertion before the 30-day follow-up visit; * Use of an intra-aortic balloon pump (IABP), extracorporeal membrane oxygenation (ECMO), or percutaneous ventricular assist devices (e.g. Impella or TandemHeart) within the last 30 days; * Confirmed diagnosis of AL amyloidosis; * Acute myocardial infarction Type 1 within 30 days of enrollment, or planned coronary revascularization in the next 30 days; * Stroke within 30 days of enrollment; * Severe Bleeding Risk (any of the following): 1. Previous intracranial bleed unless there is documentation in the medical record (from a physician that is not part of the study) that the patient can safely use anticoagulation for 7 days, 2. GI bleeding within 6 months requiring hospitalization and/or transfusion, 3. Recent major surgery within 30 days if the surgical wound is judged to be associated with an increased risk of bleeding, 4. Procedure with arterial ilio-femoral access \> 6 FR within 30 days, 5. Platelet count \<75,000 cells/mm3, 6. Uncorrectable bleeding diathesis or coagulopathy (e.g. INR ≥2 not due to anticoagulation therapy) or hypercoaguable state including HIT; 7. Inability to tolerate anticoagulation therapy for up to 7 days. * Contraindicated Anatomy : 1. Descending aortic anatomy that would prevent safe placement of the device \[\<18 mm or \>31 mm aorta diameter at deployment location (measured between the superior aspect of the T10 vertebra and superior aspect of the L1 vertebra)\], 2. Ilio-femoral diameter or peripheral vascular anatomy that would preclude safe placement of a 21F (outer diameter) introducer sheath, 3. Femoral artery depth inconsistent with use of closure device, 4. Abnormalities or severe vascular disease that would preclude safe access and device delivery (e.g. aneurysm with thrombus, marked tortuosity, significant narrowing or inadequate size of the abdominal aorta, iliac or femoral arteries, or severe calcification), 5. Known connective tissue disorder (e.g. Marfan Syndrome) or other aortopathy at risk of vascular injury, 6. Any endovascular stent graft in the descending aorta. Any endovascular stent graft in the femoro-iliac vessels that is not well endothelialized and would preclude safe introduction/removal of the Aortix pump as demonstrated by imaging. * Known hypersensitivity or contraindication to study or procedure medications (e.g. anticoagulation therapy) or device materials (e.g. history of severe reaction to nickel or nitinol); * Participation in any other clinical investigation that is likely to confound study results or affect the study; * Poor health such that the patient is unable to undergo the Aortix device placement/retrieval and/or unlikely to be able to survive to the 30-day visit; * Unable or unwilling to undergo screening (imaging, PA Catheter placement), device implant and retrieval procedures or return for 30-day visit. Inclusion Criteria (Advanced Heart Failure Registry): * Currently admitted to the hospital with a primary diagnosis of decompensated HF, irrespective of ejection fraction (EF). * Patient has already been evaluated and indicated to receive an LVAD or heart transplant and will receive the LVAD or be listed for heart transplantation in the next 30 days if their congestion status and renal function improves. * Patient must have been treated with ≥ 80 mg IV furosemide bid or equivalent and have evidence of increasing diuretic dosing requirements over the past 12 months, as tolerated. * Must have evidence of refractoriness to medical management as documented by persistent signs and/or symptoms of congestion as evidenced by at least 2+ pitting edema, elevated jugular venous pressure \>12 cm water, or ascites after treatment with IV diuretics for a minimum of 24 hours. * Serum creatinine ≥ 2.0 mg/dL AND eGFR ≤ 45 ml/min/1.73m2 at time of enrollment * Age ≥ 21 years and able to provide written informed consent. * Negative pregnancy test if patient is of childbearing potential. Exclusion Criteria (Advanced Heart Failure Registry): * Treatment with high dose IV inotropes within 48 hours prior to enrollment. High dose is defined as any one of the following: \>5 µg/kg/min dopamine OR \>5 µg/kg/min dobutamine OR \>0.375 µg/kg/min milrinone. * Active and ongoing hypotension with a systolic blood pressure \<80 mmHg lasting more than 30 minutes or a mean arterial pressure (MAP) \<55 mmHg lasting more than 30 minutes at enrollment. * Treatment with vasopressors (defined as phenylephrine, norepinephrine, epinephrine or, vasopressin) within 48 hours prior to enrollment. * An estimated PASP of \>80 mmHg as measured on echocardiogram or echocardiographic evidence of primarily right heart failure. * Acute kidney failure defined as an increase in serum creatinine to ≥ 4.0mg/dL at enrollment. * Evidence of contrast-induced nephropathy, nephritis, or nephrotic syndrome. * Prior kidney transplant, single kidney, partial nephrectomy OR use of dialysis, continuous renal replacement therapy (CRRT), or ultrafiltration in the last 90 days prior to enrollment. * Confirmed decompensated cirrhosis (defined as Child Pugh class B or C) or concern for shock liver (AST \> 1000U/L or total Bilirubin \> 5.0mg/dl) at enrollment. * Presence of an active, uncontrolled infection that would preclude safe placement or removal of the device. * Current or previous support with a durable LVAD. * INTERMACS Profile 1 at enrollment. * Currently on mechanical ventilatory support. * Use of an extracorporeal membrane oxygenation (ECMO) or percutaneous ventricular assist device (e.g., Impella or TandemHeart) within the last 30 days. * Confirmed diagnosis of AL amyloidosis. * Acute myocardial infarction Type 1 within 30 days of enrollment or planned coronary revascularization in the next 30 days. * Stroke within 30 days of enrollment. * Severe Bleeding Risk (any of the following): * Previous intracranial bleed unless there is documentation in the medical record (from a physician that is not part of the study) that the patient can safely use anticoagulation for 7 days. * GI bleeding within 6 months requiring hospitalization and/or transfusion. * Recent major surgery within 30 days if the surgical wound is judged to be associated with an increased risk of bleeding. * Procedure with arterial ilio-femoral access \> 6 Fr within 30 days. * Platelet count \<75,000 cells/mm3 . * Uncorrectable bleeding diathesis or coagulopathy (e.g., INR≥ 2 not due to anticoagulation therapy) or hypercoagulable state including HIT. * Inability to tolerate anticoagulation therapy for up to 7 days. * Contraindicated Anatomy : * Descending aortic anatomy that would prevent safe placement of the device \[\<18 mm or \>31 mm aorta diameter at deployment location (measured between the superior aspect of the T10 vertebra and superior aspect of the L1 vertebra)\]. * Ilio-femoral diameter or peripheral vascular anatomy that would preclude safe placement of a 21 Fr (outer diameter) introducer sheath. * Femoral artery depth inconsistent with use of closure device. * Abnormalities or severe vascular disease that would preclude safe access and device delivery (e.g., aneurysm with thrombus; marked tortuosity; significant narrowing or inadequate size of the abdominal aorta, iliac, or femoral arteries; or severe calcification). * Known connective tissue disorder (e.g., Marfan Syndrome) or other aortopathy at risk of vascular injury. * Any endovascular stent graft in the descending aorta. Any endovascular stent graft in the femoro-iliac vessels that is not well endothelialized and would preclude safe introduction/removal of the Aortix pump as demonstrated by imaging. * Known hypersensitivity or contraindication to study or procedure medications (e.g., anticoagulation therapy) or device materials (e.g., history of severe reaction to nickel or nitinol). * Participation in any other clinical investigation that is likely to confound study results or affect the study. * Poor health such that the patient is unable to undergo the Aortix device placement/retrieval and/or unlikely to be able to survive to the 30-day visit. * Unable or unwilling to undergo screening, device implant and retrieval procedures, or return for 30-day visit.

Idoneità in frasi semplici

I criteri di questa scheda non sono ancora stati suddivisi in affermazioni distinte. Il testo del registro qui sopra è completo ed è la versione autorevole.

Disegno dello studio

Disegno dello studio
Tipo di studio	Interventistico
Fase	Non applicabile
Assegnazione	Randomizzata
Modello di intervento	PARALLEL
Finalità principale	TREATMENT
Mascheramento	NONE (0)
Arruolamento	320 partecipanti ricercati

Sponsor e collaboratori

Procyrion Sponsor

Bracci e interventi

Treatment ArmEXPERIMENTAL
Eligible ADHF patients with diuretic resistance (irrespective of ejection fraction) will be enrolled and randomized 2:1 to either the Aortix system or standard of care medical management. Randomization will be stratified by ejection fraction.
Control ArmNO_INTERVENTION
The Control arm should receive standard of care therapy as per the study directed Diuretic Care Treatment Algorithm.
Advanced HF RegistryEXPERIMENTAL
For the Advanced HF registry, all eligible enrolled subjects will receive Aortix system support.

Interventi

Dispositivo Aortix System
Aortix is a circulatory support device for chronic heart failure patients on medical management who have been hospitalized for acute decompensated heart failure (ADHF) and are resistant to diuretic therapy.

Esiti misurati

Esito primario
Primary Safety Endpoint: Incidence of Aortix Device / Procedural-Related Major Adverse Events (MAE) through 30 days of Follow-up.
Incidence of Major Adverse Events
Orizzonte temporale Baseline to 30 day Follow-Up
Esito primario
Primary Effectiveness Endpoint: Combined composite of clinically significant reduction in net fluid loss over 7 days and freedom from mortality or heart failure re-hospitalization/therapy escalation from the baseline visit to the 30-day follow-up visit.
Composite of net fluid loss, mortality and HF hospitalization/escalation of therapy
Orizzonte temporale Baseline to 30 day Follow-Up
Esito secondario
Net Fluid Loss
Change in Net Fluid Loss from Baseline to Day 7/Discharge
Orizzonte temporale Baseline to Day 7
Esito secondario
All-cause Mortality
Rate of mortality
Orizzonte temporale Baseline to 30 day Follow-Up
Esito secondario
HF Re-Hospitalization or escalation of HF therapy
Evaluation of HF re-hospitalization and therapy escalation
Orizzonte temporale Baseline to 30 day Follow-Up
Esito secondario
eGFR
Evaluation of changes in eGFR
Orizzonte temporale Baseline to 30 day Follow-Up
Esito secondario
NT-proBNP
Evaluation of NT-proBNP
Orizzonte temporale Baseline to 30 day Follow-Up
Esito secondario
Patient Reported Dyspnea Assessment
Change in patient reported dyspnea scale
Orizzonte temporale Baseline to 30 day Follow-Up
Esito secondario
Standing body weight
Change in standing body weight
Orizzonte temporale Baseline to 30 day Follow-Up
Esito secondario
Incidence and percentages of major adverse events (MAE) Pooled
Incidence and percentages of major adverse events (MAE) pooled analysis of Aortix randomized cohort and registry cohort
Orizzonte temporale Baseline to 30 day Follow-Up

Date

Date
Data di inizio	23 agosto 2023 (effettiva)
Conclusione primaria	1 gennaio 2028 (stimata)
Conclusione	1 agosto 2028 (stimata)
Prima pubblicazione	10 gennaio 2023 (effettiva)
Ultimo aggiornamento	25 agosto 2026
Risultati pubblicati	Non indicato nella scheda del registro
Stato verificato l'ultima volta	agosto 2026

«Effettiva» significa che l'evento è avvenuto. «Stimata» significa che lo sponsor lo prevede. Le due cose non sono equivalenti.

Centri

33 centri stanno reclutando

Hungary

Hungary
Struttura	Città	Stato o regione	Stato
Semmelweis University	Budapest		In reclutamento

United States

United States
Struttura	Città	Stato o regione	Stato
Jefferson Abington Hospital	Abington	Pennsylvania	In reclutamento
AnMed Health	Anderson	South Carolina	In reclutamento
University of Michigan, Cardiovascular Medicine	Ann Arbor	Michigan	Ritirato
Emory University Hospital	Atlanta	Georgia	In reclutamento
Piedmont Healthcare Inc.	Augusta	Georgia	In reclutamento
New York Presbyterian - Brooklyn Methodist Hospital	Brooklyn	New York	In reclutamento
Atrium Health Sanger Heart and Vascular Institute	Charlotte	North Carolina	In reclutamento
University of Virginia	Charlottesville	Virginia	Interrotto
University of Chicago	Chicago	Illinois	In reclutamento
Advocate IMMC	Chicago	Illinois	In reclutamento
The Ohio State University	Columbus	Ohio	In reclutamento
John Muir Health	Concord	California	In reclutamento
Henry Ford	Detroit	Michigan	In reclutamento
Advocate Aurora - Good Samaritan	Downers Grove	Illinois	Interrotto
Duke University Medical Center	Durham	North Carolina	Attivo, non in reclutamento
Ascenscion Alexian Brothers	Elk Grove Village	Illinois	In reclutamento
Broward Health	Fort Lauderdale	Florida	In reclutamento
Baylor Scott & White	Fort Worth	Texas	Ritirato
Hackensack University Medical Center	Hackensack	New Jersey	In reclutamento
Texas Heart Institute	Houston	Texas	In reclutamento
University of Mississippi Medical Center	Jackson	Mississippi	In reclutamento
Wellstar Research Institue	Marietta	Georgia	Interrotto
Intermountain Health	Murray	Utah	Ritirato
Jersey Shore University Medical Center	Neptune City	New Jersey	In reclutamento
Nyph/Cumc	New York	New York	In reclutamento
Northwell Health (Lenox Hill)	New York	New York	Interrotto
Mount Sinai Morningside	New York	New York	In reclutamento
Oklahoma Cardiovascular Research Group	Oklahoma City	Oklahoma	In reclutamento
Ascension Sacred Heart	Pensacola	Florida	Ritirato
Thomas Jefferson University Hospital	Philadelphia	Pennsylvania	Ritirato
Penn Presbyterian Medical Center	Philadelphia	Pennsylvania	In reclutamento
Mayo Clinic - Arizona	Phoenix	Arizona	In reclutamento
Banner--University Medical Center Phoenix	Phoenix	Arizona	In reclutamento
Baylor Scott & White	Plano	Texas	Ritirato
Oregon Health & Sciences University	Portland	Oregon	Attivo, non in reclutamento
Nuvance Health	Poughkeepsie	New York	In reclutamento
Virginia Commonwealth University	Richmond	Virginia	In reclutamento
San Francisco Veterans Administration	San Francisco	California	Interrotto
University of California San Francisco	San Francisco	California	In reclutamento
Zuckerberg San Francisco General	San Francisco	California	In reclutamento
HonorHealth Medical Center	Scottsdale	Arizona	Interrotto
Northwell Health (Staten Island)	Staten Island	New York	In reclutamento
Tallahassee Research Institute	Tallahassee	Florida	Interrotto
AdventHealth Tampa	Tampa	Florida	In reclutamento
BayCare Medical/St. Joseph's Hospital	Tampa	Florida	In reclutamento
University of South Florida	Tampa	Florida	In reclutamento
Cleveland Clinic Florida	Weston	Florida	In reclutamento
Ascension via Christi Kansas	Wichita	Kansas	Interrotto
Novant Health New Hanover Regional Medical Center	Wilmington	North Carolina	Ritirato

Documenti dello studio

In questa scheda del registro non sono collegati documenti.

Modifiche nel tempo

25 agosto 2026
Centro aggiunto
1 site added (50 total)
4950
4 agosto 2026
Data di conclusione posticipata
Primary completion delayed 365 days
2027-01-012028-01-01

Registro: ClinicalTrials.gov · NCT########

https://xmedica.io/trials/ctgov/NCT05677100