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NCT00782639 · ClinicalTrials.gov registry record · Phase 4

Renal Safety of Iopamidol Versus Iodixanol During Coronary Angiography in Diabetic Patients

A Phase 4 study, sponsored by Bracco Diagnostics.

Terminated
Registry status
Phase 4
Development phase
23
Enrollment target

NCT00782639: Clinical Trial Phase 4 study, sponsored by Bracco Diagnostics.

NCT00782639 is a Phase 4 study that was terminated before completion, run by Bracco Diagnostics. The registered enrollment target is 23 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00782639, a Phase 4 study, was terminated before completion, sponsored by Bracco Diagnostics.

TERMINATED
Registry status
Phase 4
Development phase
23 participants
Enrollment target

Study Summary

The purpose of this study is to compare the incidence of contrast-induced nephropathy (CIN) following the administration of iopamidol-370 (Iopamiro-370) and iodixanol-320 (Visipaque 320) in patients with moderate-to-severe chronic kidney disease and diabetes mellitus undergoing cardiac angiography.

Primary Outcome

The number of participants who presented with CIN (defined as an increase in Serum Creatinine (SCr) from baseline greater than or equal to 0.5 mg/dL following the administration of iopamidol-370 or iodixanol 320 while undergoing cardiac angiography). Since CIN is a prospectively-defined outcome measure of the trial, patients experiencing CIN were not reported as having an adverse event.

Interventions

  • DRUG iodixanol
  • DRUG Iopamidol injection 76%

Trial Details

FieldValue
Enrollment Target 23 participants
Start Date 2009-03
Est. Completion 2009-09
Phase Phase 4
Bracco Diagnostics

37 total trials

Why NCT00782639 stopped before completion

NCT00782639 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 23 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (96% lower).

The record links to 0 conditions, and to 2 interventions - of which iodixanol is the first listed.

NCT00782639 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00782639 about?

NCT00782639 is a clinical study titled "Renal Safety of Iopamidol Versus Iodixanol During Coronary Angiography in Diabetic Patients". The purpose of this study is to compare the incidence of contrast-induced nephropathy (CIN) following the administration of iopamidol-370 (Iopamiro-370) and iodixanol-320 (Visipaque 320) in patients with moderate-to-severe chronic kidney disease and diabetes mellitus undergoing cardiac angiography.

What is the current status of trial NCT00782639?

This trial is currently terminated. It is a Phase 4 study. The enrollment target is 23 participants. The study started on 2009-03. Estimated completion is 2009-09.

What interventions are being tested in trial NCT00782639?

The interventions under investigation include: iodixanol (DRUG), Iopamidol injection 76% (DRUG).

Who is sponsoring clinical trial NCT00782639?

This trial is sponsored by Bracco Diagnostics, which has 37 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00782639's enrollment target sits among peer trials

23 1725th of 2000 higher than 270 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 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 NCT00782639, the US trial registry maintained by the National Library of Medicine. NCT00782639 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.