Effects of Allopurinol on Diastolic Function in Chronic Heart Failure Patients

Sponsor
Universita di Verona (Other)
Overall Status
Completed
CT.gov ID
NCT00477789
Collaborator
(none)
1

Study Details

Study Description

Brief Summary

In patients with chronic heart failure (CHF)due to dilated cardiomyopathy diastolic dysfunction occurs frequently and is related to a poor outcome. We have previously shown that parameters of diastolic function significantly correlate with uric acid levels, a marker of impaired oxidative metabolism. We aimed to determine whether inhibition of xanthine oxidase with allopurinol might affect diastolic function in patients with CHF.

Condition or Disease Intervention/Treatment Phase
Phase 4

Study Design

Study Type:
Interventional
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double
Primary Purpose:
Treatment
Official Title:
Effects of Allopurinol on Diastolic Function in Chronic Heart Failure Patients

Outcome Measures

Primary Outcome Measures

  1. diastolic function uric acid levels BNP [three months]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • chronic heart failure;

  • left ventricular systolic dysfunction (ejection fraction <45%)

  • stable clinical conditions in the previous three months

  • optimal medical therapy for CHF

  • normal sinus rhythm

  • written informed consent

  • age >18 years

Exclusion Criteria:
  • renal failure (s-creatinine >2.5 mg/dl)

  • already on allopurinol

  • malignancies

  • chronic inflammatory diseases

Contacts and Locations

Locations

Site City State Country Postal Code
1 Division of Cardiology, University Hospital of Verona Verona Italy 37129

Sponsors and Collaborators

  • Universita di Verona

Investigators

  • Principal Investigator: Mariantonietta Cicoira, MD, PhD, Division of Cardiology, University of Verona, Italy

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00477789
Other Study ID Numbers:
  • 802
First Posted:
May 24, 2007
Last Update Posted:
May 24, 2007
Last Verified:
May 1, 2007
Keywords provided by , ,
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 24, 2007