Pilot Study Lp299v Supplementation in Chronic Heart Failure
Heart Failure, Heart Failure With Reduced Ejection Fraction, Heart Failure, Systolic
About this trial
This is an interventional basic science trial for Heart Failure focused on measuring Endothelial Function, Microbiome, Heart Failure, Ejection Fraction
Eligibility Criteria
Inclusion Criteria: Age between 21-89 years old Clinical diagnosis of Congestive Heart Failure (CHF) in the six months prior to enrollment along with an echocardiogram documenting systolic dysfunction with ejection fraction ≤40% Clinical diagnosis of CHF in the six months prior to enrollment along with an echocardiogram documenting diastolic dysfunction with an ejection fraction ≥50%, and a H2FpEFF score of ≥6 New York Heart Association (NYHA) Class II-IIID heart failure symptoms with either ischemic or non-ischemic etiology OR similar diagnosis with congestive heart failure (CHF) along with an echocardiogram documenting an LV ejection fraction of 50% or more with similar NYHA classification as those with LVEF of 40% or less Evidence of systemic inflammation at baseline (C-reactive protein ≥ 2 mg/L at the time of screening) Exclusion Criteria: Heart failure due to severe valve disease such as Aortic Stenosis, Mitral Regurgitation, or Mitral Stenosis Cancer besides non-melanoma skin carcinomas or localized prostate and breast cancer at the time of enrollment with life expectancy <1 year Lung disease such as Chronic Obstructive Pulmonary Disease (COPD), emphysema, or Pulmonary fibrosis Active inflammatory disease or infectious disease at the time of enrollment Current treatment (or use within the past 14 days) of steroids or anti-inflammatory treatments (excluding non-steroidal anti-inflammatory medications or steroids used solely for IV contrast dye allergy) Chronic Kidney Disease with eGFR ≤ 30 mL/min Hepatic Failure (Child's Class B or C) Patients with Gastrointestinal (GI) tract illness such as short gut syndrome, inflammatory bowel disease, or an ileostomy, such that probiotic absorption would be altered Anticipated need for cardiac surgery during the projected study period for the subject Pregnancy Patients who are receiving Vitamin K antagonists such as Coumadin or Warfarin Neutropenia (Absolute Neutrophil Count (ANC) < 1800/mm3) Inability to give informed consent or follow the study protocol On antibiotics at the time of enrollment or within one month of enrollment Currently taking a Lactobacillus based probiotic as an outpatient at the time of enrollment Patients who are unable to walk on treadmill or use a bicycle to participate in exercise testing Allergy to Lp299v probiotic supplement
Sites / Locations
- Medical College of WisconsinRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Placebo Comparator
Lp299v
Placebo Control
Subjects will consume 20 billion colony forming units of Lp299v (2 capsules) once daily for 12 weeks.
Subjects will consume potato starch (2 capsules) once daily for 12 weeks.