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Completed Phase 3 Interventional Results available

A Multicenter Clinical Trial of Allopurinol to Prevent Kidney Function Loss in Type 1 Diabetes

ClinicalTrials.gov ID: NCT02017171

Public ClinicalTrials.gov record NCT02017171. 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 4, 2026, 12:21 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

PERL: A Multicenter Clinical Trial of Allopurinol to Prevent GFR Loss in T1D

Brief summary

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

Despite improvements during the past 20 years in blood glucose and blood pressure control, diabetic kidney disease remains one of the most important causes of health problems in patients with diabetes. Novel treatments to complement blood glucose and blood pressure control are urgently needed. The goal of this study is to see whether a medication called allopurinol may help prevent loss of kidney function among people with type 1 diabetes. Allopurinol has been used for many years to decrease high blood uric acid and treat gout - a disease characterized by arthritis, especially of the foot joints. There is evidence suggesting that allopurinol might also be useful in people with diabetes who have normal or moderately impaired kidney function to decrease the risk of developing advanced kidney disease in the future. To prove this beneficial effect of allopurinol, we will be conducting an international clinical trial at eight diabetes centers, enrolling approximately 480 patients with type 1 diabetes who are at increased risk of developing kidney disease. Participants will be randomly assigned to take allopurinol or placebo (inactive pill) for three years, during which they will be followed through periodical visits. To prevent any possible bias, neither the participants nor the clinical staff knows who is taking allopurinol and who is taking the placebo. Kidney function will be measured at the beginning and at the end of the treatment period to see whether patients taking allopurinol experience a slower loss of kidney function over time as compared to those taking the inactive pill. If this trial is successful, the reduction in health problems resulting from the prevention or delay of kidney function loss due to the use of allopurinol would have a major impact on the lives of type 1 diabetic patients as well as on society at large, significantly reducing the human and financial costs associated with diabetic kidney disease. Because of the emphasis on early intervention, the proposed trial, if successful, will establish a new paradigm in treatments to slow or prevent progression towards end stage kidney disease in type 1 diabetes far beyond anything achieved to date.

Study identification

NCT ID
NCT02017171
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Alessandro Doria
Other
Enrollment
530 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 70 Years
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
Jan 31, 2014
Primary completion
Jul 14, 2019
Completion
Aug 30, 2019
Last update posted
Dec 3, 2020

2014 – 2019

United States locations

U.S. sites
23
U.S. states
11
U.S. cities
18
Facility City State ZIP Site status
Barbara Davis Center / University of Colorado Denver Aurora Colorado 80045
Kaiser Permanente Colorado Institute of Health Research Denver Colorado 80231
Emory University - Grady Memorial Hospital Atlanta Georgia 30303
Atlanta Diabetes Associates Atlanta Georgia 30318
Northwestern University Feinberg School of Medicine Chicago Illinois 60611
Massachusetts General Hospital Boston Massachusetts 02114
Joslin Diabetes Center Boston Massachusetts 02215
University of Massachusetts Memorial Health Care Worcester Massachusetts 01655
Brehm Center for Diabetes Research / University of Michigan Ann Arbor Michigan 48105
Henry Ford Health System Detroit Michigan 48202
University of Minnesota Minneapolis Minnesota 55455
Washington University St Louis Missouri 63110
Winthrop-University Hospital Mineola New York 11501
ICAHN School of Medicine at Mount Sinai New York New York 10029
Weill Cornell Medical Center New York New York 10065
SUNY Upstate Medical University Syracuse New York 13210
Albert Einstein College of Medicine / Montefiore Medical Center The Bronx New York 10461
Jacobi Medical Center The Bronx New York 10461
University of Texas Southwestern Dallas Texas 75390
Virginia Mason Medical Center Seattle Washington 98101
University of Washington Seattle Washington 98105
Providence Sacred Heart Medical Center Spokane Washington 99204
Gunderson Health System La Crosse Wisconsin 54601

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 7 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02017171, 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 Dec 3, 2020 · Synced Sep 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02017171 live on ClinicalTrials.gov.

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