Status:

TERMINATED

The Effect of Ribose on B-Type Natriuretic Peptide (BNP) Levels in Congestive Heart Failure Patients

Lead Sponsor:

Valen Labs

Conditions:

Congestive Heart Failure

Eligibility:

All Genders

18-80 years

Phase:

NA

Brief Summary

The purpose of this research study is to test the effectiveness of CORvalen, a medical food, to increase cellular energy sufficiently to change or modify BNP levels in congestive heart failure patient...

Detailed Description

B-type natriuretic peptide (BNP), is a blood test commonly used to track the progress of congestive heart failure. CORvalen, a medical food, contains D-Ribose (ribose), a natural substance that has be...

Eligibility Criteria

Inclusion

  • Inclusion Criteria:
  • Symptomatic adults, M/F, between 18 and 80 years of age
  • BNP levels equal to or greater than 300 pg/ml.
  • Primary or secondary diagnosis of congestive heart failure at the time of admission (any NYHA Class)
  • Diagnosis of congestive heart failure for at least 3 months
  • Able to perform 6 minute hall walk
  • No therapeutic pharmaceutical class changes for at least 1 month
  • Provide informed consent
  • A 30-day washout period must be achieved for any patient involved in a previous clinical study.
  • Exclusion
  • Insulin dependent diabetes (Type I)
  • History of obstructive valvular disease
  • History of pulmonary hypertension within the last 3 months
  • History of hypertrophic or alcoholic cardiomyopathy
  • History of restrictive cardiomyopathy
  • History of reversible cardiomyopathy
  • History of non-compliance
  • Pregnancy
  • Current enrollment in any other clinical study

Exclusion

    Key Trial Info

    Start Date :

    June 1 2006

    Trial Type :

    INTERVENTIONAL

    End Date :

    July 1 2007

    Estimated Enrollment :

    120 Patients enrolled

    Trial Details

    Trial ID

    NCT00329485

    Start Date

    June 1 2006

    End Date

    July 1 2007

    Last Update

    August 2 2007

    Active Locations (1)

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    1

    See list of Study Principal Investigators

    Columbus, Ohio, United States