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Completed Phase 2 Interventional Results available

Using Allopurinol to Relieve Symptoms in Patients With Heart Failure and High Uric Acid Levels

ClinicalTrials.gov ID: NCT00987415

Public ClinicalTrials.gov record NCT00987415. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 3, 2026, 8:54 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Xanthine Oxidase Inhibition for Hyperuricemic Heart Failure Patients

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to determine whether allopurinol is effective in relieving symptoms of patients with heart failure and high blood uric acid levels.

Study identification

NCT ID
NCT00987415
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Duke University
Other
Enrollment
253 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 30, 2010
Primary completion
Nov 30, 2013
Completion
May 31, 2014
Last update posted
Nov 3, 2014

2010 – 2014

United States locations

U.S. sites
9
U.S. states
8
U.S. cities
9
Facility City State ZIP Site status
Morehouse School of Medicine Atlanta Georgia
Harvard University Boston Massachusetts
University of Minnesota Minneapolis Minnesota
Mayo Clinic Rochester Minnesota
Duke University Medical Center Durham North Carolina
University Hospitals-Case Medical Center Cleveland Ohio 44106
Baylor College of Medicine Houston Texas
Univ. of Utah Health Sciences Center Salt Lake City Utah
University of Vermont Burlington Vermont

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00987415, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 3, 2014 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00987415 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →