Clinical Trials Directory

Trials / Completed

CompletedNCT01525888

Renin-angiotensin-aldosterone System (RAAS) Blockade and Contrast Induced Nephropathy

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
100 (actual)
Sponsor
Soroka University Medical Center · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The aim of the current study is to evaluate prospectively whether concomitant administration of renin-angiotensin-aldosterone system (RAAS) blockers (namely ACE-I and ARBs') influence the change in estimated glomerular filtration rate or GFR (eGFR) after administration of contrast media in patients undergoing non-emergent coronary angiography.

Detailed description

Contrast-induced nephropathy (CIN) is defined as an absolute or relative increase in serum creatinine compared to the baseline values, together with exposure to a contrast agent and exclusion of alternative explanations for renal impairment. Most frequently the renal impairment develops 48 hours post exposure. Although RAAS blocking agents are widely used among patients requiring contrast studies, data regarding the effect of these agents on the development of CIN are sparse and inconsistent. Patients undergoing percutaneous coronary intervention are frequently treated with RAAS blocking agents. Despite the not infrequent occurrence of CIN following percutaneous coronary intervention (PCI) no guidelines are available on the topic of the cessation of the RAAS inhibitors prior to the procedure.

Conditions

Interventions

TypeNameDescription
PROCEDUREstop angiotensin converting enzyme inhibitor or angiotensin receptor blocker (ACE-I/ARB)stoping for 6 days treatment with angiotensin converting enzyme inhibitor or angiotensin receptor blocker

Timeline

Start date
2012-02-01
Primary completion
2013-12-01
Completion
2013-12-01
First posted
2012-02-03
Last updated
2015-06-08

Source: ClinicalTrials.gov record NCT01525888. Inclusion in this directory is not an endorsement.