The Impact of Pomegranate Extract on Chronic Cardiomyopathy Complicated by Renal Insufficiency (ImPrOVE): a Pilot Study

Jennifer Cowger , MD, MS

Status and phase: Terminated; Phase 2

Conditions: Cardiomyopathy; Heart Failure

Treatments: Drug: Sugar Pill; Drug: POMx, pomegranate polyphenol extract

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT01102140

IMPROVEHF

Details and patient eligibility

About

This blinded, controlled study will examine the impact of pomegranate polyphenol extract (POMx, from Pom Wonderful, LLC), 1000mg on cardiomyopathy in subjects with chronic renal insufficiency.

Full description

Heart failure (HF) is a disease of great prevalence in the U.S. with an associated high morbidity and mortality. In individuals with concomitant chronic renal insufficiency (CRI), outcomes are even worse due to pharmaceutical under treatment and higher baseline levels of oxidative stress. Reactive oxygen species (ROS) are generated during mechanoenergetic uncoupling and can cause myocardial protein, lipid, and DNA damage, leading to the development of HF. One means of preventing the progression of HF may be through ROS reduction or an improvement in systemic or local oxidative stress handling. In this randomized, single blind placebo-controlled pilot study, we hypothesize that 12 weeks of treatment with oral pomegranate extract (POMx) will lead to a reduction in oxidative stress (as assessed by measuring thiobarbituric acid-reactive substances, F8-isoprostanes, and glutathione) in subjects (n=30) with cardiomyopathy (LVEF ≤40%) and CRI (GFR <60 ml/hr). Secondary aims include assessing the impact of POMx on myocardial remodeling and endothelial dysfunction by measuring serum collagen levels and asymmetric dimethylarginine, respectively. Findings from this study will serve as pilot data for a larger randomized trial of longer term POMx therapy in subjects with cardiomyopathy.

Enrollment: 20 patients

Sex: All

Ages: 21+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Adult subjects (≥21 years of age) with cardiomyopathy (ejection fraction ≤40%) of at least 1 year duration and CRI (GFR <60 cc/hr for at least 3 months) will be eligible for enrollment.
• Subjects must have New York Heart Association (NYHA) functional class I-III symptoms and be on stable doses of HF evidence-based therapies (β-blocker, ACE inhibitor or ARBs, aldosterone inhibitor [if appropriate]) for at least 3 months or have a documented contraindication or intolerance to such therapy

Exclusion criteria

• Subjects admitted to a hospital for acute myocardial infarction (defined as positive troponins) or HF exacerbation within the last 6 months will not be eligible for enrollment.

• Subjects on warfarin or rosuvastatin will also be excluded.

• Other exclusion criteria are as follows:

  • HF that is deemed to be congenital or infiltrative in etiology
  • the presence of a life-threatening illness with a projected survival ≤6 months; ongoing infection
  • pregnancy
  • inability to follow-up
  • end-stage renal disease requiring dialysis
  • renal transplant listing
  • recent (within last 6 months) POMx use or intake >8 ounces daily of pomegranate juice
  • known hypersensitivity to any fruit in the Punicaceae family
  • connective tissue or collagen vascular disease

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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20 participants in 2 patient groups, including a placebo group

POMx

Active Comparator group

Description:

15 subjects will received 1000 mg of oral POMx for 12 weeks.

Treatment:

Drug: POMx, pomegranate polyphenol extract

Control- sugar Pill

Placebo Comparator group

Description:

15 subjects will receive a matching sugar pill for 12 weeks.

Treatment:

Drug: Sugar Pill