Viewing Study NCT00786734



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Study NCT ID: NCT00786734
Status: WITHDRAWN
Last Update Posted: 2012-03-30
First Post: 2008-11-05

Brief Title: Pitavastatin Pre-Treatment Study in Patient With Elective PCI for Stable Angina Pectoris PIPA
Sponsor: JW Pharmaceutical
Organization: JW Pharmaceutical

Study Overview

Official Title: A Randomized Open Label Comparative Study to Evaluate Effect of Pitavastatin for Reduction of Myocardial Damage in Patient Are Scheduled Elective PCI for Stable Angina Pectoris
Status: WITHDRAWN
Status Verified Date: 2012-03
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: None
Brief Summary: Patients who is scheduled elective PCI are randomized to pitavastatin 4mg daily or without pitavastatin for 5 -7days before the procedure Creatine kinase-MB troponin I and myoglobin levels are measured at baseline and at 8 and 24 hours after the procedure1st evaluation After PCI pitavastatin will be administered for additional 4 weeks2nd evaluation
Detailed Description: Procedural ischemic myocardial injury remains the most frequent complication after coronary angioplasty Recently it was reported that pretreatment with atorvastatin reduce the myocardial damage compared to placebo Thus we will evaluate the difference of pretreatment of pitavastatin compared to standard therapy on the reduction of myocardial damage in patient who is scheduled elective PCI for stable angina pectoris

Study Oversight

Has Oversight DMC: None
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?: None