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NCT00498537 · ClinicalTrials.gov registry record · NA

Spironolactone for Reducing Proteinuria in Diabetic Nephropathy

A NA study, sponsored by US Department of Veterans Affairs.

Completed
Registry status
NA
Development phase
30
Enrollment target

NCT00498537: Completed NA study, sponsored by US Department of Veterans Affairs.

NCT00498537 is a NA study that has completed, run by US Department of Veterans Affairs. The registered enrollment target is 30 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00498537, a NA study, has completed, sponsored by US Department of Veterans Affairs.

COMPLETED
Registry status
NA
Development phase
30 participants
Enrollment target

Study Summary

Introduction: Aldosterone seems to have deleterious effects on the kidneys. Many animal studies and few clinical trials now have shown that suppression of aldosterone by aldosterone receptor blockers ameliorated these effects. Method: In a double-blind, cross over study, 24 patients with diabetic nephropathy who were already receiving either ACE inhibitor(lisinopril 20-40 mg/day ) or ARB( losartan 25-100 mg/day )were given spironolactone( 25 mg during the first month and 50 mg during the second and third month if serum K remained ok) or matching placebo with 1 month of washout in between. All patients were from a single center and exclusively male veterans. Blood pressure, serum creatinine, serum K and spot urine protein/creatinine were measured at the beginning and end of each study period. The study was started in May of 2003 and completed in May 2006.

Interventions

  • DRUG spironolactone

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2003-01
Est. Completion 2006-06
Phase NA
US Department of Veterans Affairs

632 total trials

What the finished NCT00498537 record still lists

NCT00498537 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 30 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 1 intervention - of which spironolactone is the first listed.

NCT00498537 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00498537 about?

NCT00498537 is a clinical study titled "Spironolactone for Reducing Proteinuria in Diabetic Nephropathy". Introduction: Aldosterone seems to have deleterious effects on the kidneys. Many animal studies and few clinical trials now have shown that suppression of aldosterone by aldosterone receptor blockers ameliorated these effects. Method: In a double-blind, cross over study, 24 patients with diabetic n...

What is the current status of trial NCT00498537?

This trial is currently completed. It is a NA study. The enrollment target is 30 participants. The study started on 2003-01. Estimated completion is 2006-06.

What interventions are being tested in trial NCT00498537?

The interventions under investigation include: spironolactone (DRUG).

Who is sponsoring clinical trial NCT00498537?

This trial is sponsored by US Department of Veterans Affairs, which has 632 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00498537's enrollment target sits among peer trials

30 1593rd of 2000 higher than 299 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00498537, the US trial registry maintained by the National Library of Medicine. NCT00498537 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.