Clinical Trials Directory

Trials / Unknown

UnknownNCT02991742

Ioxaglate Versus Iodixanol for the Prevention of Contrast-induced Nephropathy in High-risk Patients (IDPC Trial)

Ioxaglate Versus Iodixanol for the Prevention of Contrast-induced Nephropathy in High-risk Patients After Diagnostic and Therapeutic Cardiac Catheterization (IDPC Trial)

Status
Unknown
Phase
Study type
Observational
Enrollment
2,262 (estimated)
Sponsor
Instituto Dante Pazzanese de Cardiologia · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Contrast media-induced nephropathy following diagnostic and therapeutic cardiac catheterization.

Detailed description

Contrast-induced acute kidney injury represents a serious complication of procedures requiring administration of iodinated contrast media and is associated with the need for dialysis, prolonged hospitalization, increased costs, and mortality. Contrast-induced nephropathy is defined as an increase of 25% in serum creatinine before the procedure. Iodixanol, a nonionic, dimeric, iso-osmolar contrast medium may be less nephrotoxic than low-osmolar contrast media in high-risk patients. The purpose of this study is to compare iodixanol versus ioxaglate in high risk patients between 48 and 96 hours after procedures that use contrast.

Conditions

Interventions

TypeNameDescription
OTHERcontrast mediaCompare 2 contrast media

Timeline

Start date
2016-12-01
Primary completion
2016-12-01
Completion
2020-11-01
First posted
2016-12-13
Last updated
2016-12-14

Source: ClinicalTrials.gov record NCT02991742. Inclusion in this directory is not an endorsement.