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Trials / Withdrawn

WithdrawnNCT00786734

Pitavastatin Pre-Treatment Study in Patient With Elective PCI for Stable Angina Pectoris (PIPA)

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Withdrawn
Phase
Phase 4
Study type
Interventional
Enrollment
0 (actual)
Sponsor
JW Pharmaceutical · Industry
Sex
All
Age
45 Years – 75 Years
Healthy volunteers
Not accepted

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 procedure(1st evaluation). After PCI, pitavastatin will be administered for additional 4 weeks(2nd 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.

Conditions

Interventions

TypeNameDescription
DRUGPitavastatin4mg daily for 5-7 days before Percutaneous Coronary Intervention(PCI) and 4mg daily for 28 days after PCI
DRUGPitavastatin4mg daily for 28 days after PCI

Timeline

Start date
2008-08-01
Primary completion
2009-05-01
Completion
2010-07-01
First posted
2008-11-06
Last updated
2012-03-30

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT00786734. Inclusion in this directory is not an endorsement.

Pitavastatin Pre-Treatment Study in Patient With Elective PCI for Stable Angina Pectoris (PIPA) (NCT00786734) · Clinical Trials Directory