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NCT00289029 · ClinicalTrials.gov registry record · Phase 4

A Study of Two Iodinated Contrast Agents in Renally Impaired Patients Undergoing Cardiac Angiography

A Phase 4 study, sponsored by Bracco Diagnostics.

Completed
Registry status
Phase 4
Development phase
400
Enrollment target

NCT00289029 is a Phase 4 study that has completed, run by Bracco Diagnostics. The registered enrollment target is 400 participants.

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The verdict

NCT00289029, a Phase 4 study, has completed, sponsored by Bracco Diagnostics.

COMPLETED
Registry status
Phase 4
Development phase
400 participants
Enrollment target

Study Summary

The main purpose of this study is to compare the incidence of contrast induced nephrotoxicity following the administration of Isovue or Visipaque in patients with moderate to severe renal insufficiency undergoing cardiac angiography. Serum creatinine will be measured before and up to 48-72 hours after the administration of the contrast agent to evaluate renal function.

Interventions

  • DRUG Iopamidol 370 mgI/mL

Trial Details

FieldValue
Enrollment Target 400 participants
Start Date 2005-07
Est. Completion 2006-06
Phase Phase 4

Sponsor

Bracco Diagnostics

37 total trials

What the Registry Record Tells You About NCT00289029

The ClinicalTrials.gov registry entry for NCT00289029 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 400 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Bracco Diagnostics, which has 37 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Iopamidol 370 mgI/mL is the first listed.

NCT00289029 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00289029 about?

NCT00289029 is a clinical study titled "A Study of Two Iodinated Contrast Agents in Renally Impaired Patients Undergoing Cardiac Angiography". The main purpose of this study is to compare the incidence of contrast induced nephrotoxicity following the administration of Isovue or Visipaque in patients with moderate to severe renal insufficiency undergoing cardiac angiography. Serum creatinine will be measured before and up to 48-72 hours aft...

What is the current status of trial NCT00289029?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 400 participants. The study started on 2005-07. Estimated completion is 2006-06.

What interventions are being tested in trial NCT00289029?

The interventions under investigation include: Iopamidol 370 mgI/mL (DRUG).

Who is sponsoring clinical trial NCT00289029?

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

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.