Randomized Trial for Patients With Chronic Heart Failure With Acute Decompensation

Heart Failure, Congestive Clinical Trial

Official title:

MOMENTUM: Multicenter Trial of the Orqis Medical CRS for the Enhanced Treatment of CHF Unresponsive to Medical Therapy

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT00357591
• Other study ID #: IDEG020301
• Status: Terminated
• Phase: N/A
• First received: July 25, 2006
• Last updated: December 24, 2009
• Start date: September 2004
• Est. completion date: January 2008

Study information

• Verified date: August 2009
• Source: Orqis Medical Corporation
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

The Company's proprietary products are based on Orqis Medical's hypothesis, supported by early clinical data, that increasing and maintaining continuous blood flow in the descending aorta, known as continuous aortic flow augmentation or CAFA, improves hemodynamics in heart failure patients. The clinical impact of the hemodynamic improvement is currently being evaluated to determine the effects of CAFA on stopping or reversing the progression of heart failure through three physiological effects:

• VASCULAR - Reducing systemic vascular resistance

• RENAL - Improving renal function

• CARDIAC - Reducing cardiac workload

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 200
• Est. completion date: January 2008
• Est. primary completion date: January 2008
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 90 Years

Eligibility

Inclusion Criteria:

1. Patients hospitalized due to decompensated heart failure who require IV inotropic and/or vasodilator and diuretic therapy

2. Patients receiving appropriate medical therapy for heart failure, defined as ACE inhibitors and beta blockers (all unless not tolerated or contraindicated) and diuretics, for 1 month prior to study entry

3. For at least 24 hours prior to inclusion into the study, the patient should be treated with a minimum dose of the following: dobutamine 2.5µg/kg/min or milrinone 0.3µg/kg/min or dopamine 5µg/kg/min. or nesiritide 0.01µg/kg/min or nitroglycerin 0.3 µg/kg/min or nitroprusside 0.3 µg/kg/min or a combination of any of these agents, with diuretic therapy. Doses of the above stated medications should be stable for 6 hours prior to inclusion into study. An increase in this dosage within the first 8 hours after enrollment is determined by the attending physician to be unlikely and the following definition of "not responding adequately to IV inotropic and/or vasodilator and diuretic therapy" is exhibited:

• PCWP is = 20 mmHg at time of randomization and PCWP was = 18 mmHg continuously for 24 hours or PCWP = 20 mmHg continuously for 12 hours prior to randomization.

• Cardiac Index < 2.4 L/min/m2

• There is evidence for abnormal renal function and/or diuretic resistance defined as: Serum creatinine > 1.2 mg/dL or Diuretic dosage of intravenous Furosemide = 120 mg daily, or equivalent

4. LVEF < 35%

5. Male or female 18-90 years of age

6. If female, no child-bearing potential or negative pregnancy test

7. Written informed consent

8. Willingness to participate in required follow-up exams

Exclusion Criteria:

1. Acute Q-wave myocardial infarction within past 7 days

2. Post cardiotomy shock within past 30 days

3. Cardiac surgery within past 14 days

4. Bridge to transplant

5. History of severe COPD as defined as FEV1 < 1.0 liter

6. History of malignant arrhythmias defined as either:

• sustained ventricular tachycardia > 15 beats or more in length, not associated with a correctable cause, within the preceding 3 months, unless the patient presently has an implantable cardiac defibrillator.

• history of ventricular fibrillation or sudden death, unless the patient presently has an implantable cardiac defibrillator

7. Patients implanted with a resynchronization device within the previous 14 days or if there is a possibility of implant within 60 days following randomization

8. Systolic pressure <80 mmHg

9. Requiring cardiopulmonary support type devices

10. Platelets < 50,000/mm3 or other evidence of coagulopathy, INR greater than 1.5 in the absence of anticoagulation therapy.

11. Infection (WBC = 12.5 x 103/ml, and or temperature = 100.5°F/38°C)

12. History of cerebral vascular accident (CVA) or transient ischemic attacks (TIA) within the last 3 months

13. Unwilling or unable to receive blood transfusion

14. Inability to undergo treatment with heparin

15. Patients on dialysis or serum creatinine > 4.0 mg/dl

16. Primary liver disease with bilirubin, SGOT, or SGPT > 4X upper limit of normal

17. Life expectancy from other disease < 12 months

18. Patients who are active on the cardiac transplantation waiting list, unless there is a documented reason (large body habitus, highly sensitized, O blood group) to anticipate that transplant is unlikely within the subsequent 65 days.

19. Symptomatic patent foramen ovale or intracardiac shunt

20. Patients diagnosed with clinically significant peripheral vascular disease, defined as absent pedal pulse or signs or symptoms of limb ischemia, including a history of intermittent claudication

21. Patients with amyloidosis, thyroid induced heart failure, high output failure secondary to an arterio-venous fistula, and significant uncorrected primary valvular disease (with the exception of mitral regurgitation believed secondary to LV dilatation)

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Heart Failure
• Heart Failure, Congestive

Intervention

Device:
• Continuous Aortic Flow Augmentation
1.0-1.5 lpm augmented blood flow

Locations

Country	Name	City	State
United States	University of California at San Diego	San Diego	California

Sponsors (1)

Lead Sponsor	Collaborator
Orqis Medical Corporation

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Alive, Number of days out of the hospital, not on mechanical assistance over 35 day period.		35 days	Yes

External Links

•   MOMENTUM Trial Website