Viewing Study NCT00736866


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Study NCT ID: NCT00736866
Status: COMPLETED
Last Update Posted: 2010-07-12
First Post: 2008-08-14
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: The Acetylcysteine for Contrast-Induced Nephropathy Trial
Sponsor: Hospital do Coracao
Organization:

Study Overview

Official Title: A Pragmatic Randomized Clinical Trial Evaluating the Effect of Acetylcysteine for Contrast-induced Nephropathy
Status: COMPLETED
Status Verified Date: 2008-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: ACT
Brief Summary: The purpose of this study is to evaluate the efficacy of acetylcysteine compared to placebo for the contrast-induced nephropathy prevention, between 48 and 96 hours after procedures that use contrast.

Contrast-induced nephropathy is defined as an increase of 25% in serum creatinine before the procedure.
Detailed Description: None

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: