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Prevention of Contrast Induced Nephropathy in Patients With Advanced Renal Dysfunction Undergoing Coronary Interventions

The Efficacy of a New Protocol for Preventing Contrast Induced Nephropathy in Patients With Advanced Renal Dysfunction Undergoing Coronary Interventions

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02468401
Enrollment
30
Registered
2015-06-10
Start date
2015-09-30
Completion date
2016-08-31
Last updated
2016-11-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ischemic Heart Disease, Kidney Disease, Chronic

Brief summary

There is a pressing need to find effective strategies for the prevention of contrast induced nephropathy in patients with advanced renal dysfunction. The current study was designed to assess the efficacy of a new protocol for preventing contrast induced nephropathy in patients with advanced renal dysfunction undergoing coronary interventions

Interventions

PROCEDUREPercutaneous coronary intervention

Patients planned for coronary angiography or percutaneous coronary intervention will be managed using a protocol that allows us to use minimal volumes of contrast dye

Sponsors

Meir Medical Center
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

Patients with estimated glomerular filtration rate\<45ml/min undergoing coronary angiography due to one of the following indications in accordance with the 2014 guidelines: 1. Elective coronary angiography due to symptoms suggestive for angina with a positive non-invasive ischemia assessment of ≥10% of left ventricle. 2. Non ST-elevation acute coronary syndrome with a GRACE score\>110

Exclusion criteria

* Patients on dialysis or those planned for dialysis in the next 3 months. * Patients with ST-elevation myocardial infarction * No symptoms or signs of heart failure * Treatment with IV diuretics during the 48 hours prior to enrolment * Patients with acute renal failure (Creatinine raise of at least 0.3mg/dl from )baseline * Patients post coronary artery bypass surgery

Design outcomes

Primary

MeasureTime frameDescription
Changes in glomerular filtration rate following coronary angiography or intervention24 and 48 hours post procedureSignificant changes are defined as a reduction ≥25% in glomerular filtration rate

Countries

Israel

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026