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Registry of Effects of high-dose statins on Contrast induced nephropathy in patients of Acute Myocardial Infarctio

Not Applicable
Recruiting
Conditions
Diseases of the circulatory system
Registration Number
KCT0003703
Lead Sponsor
Kangbuk Samsung Medical Center
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
460
Inclusion Criteria

[Inclusion Criteria]
1) Male and Female aged 20 or over
2) Non-ST elevation MI or STEMI
3) Atorvastatin(40mg) or Rosuvastatin(20mg) used for the reduction of cholesterol
4) High-intensity statin(atorvastatin 40mg, 80mg, rosuvastatin 20mg) never used or statin-naive
**Including intensity of below moderate statin.
(moderate intensity statins: rosuvastatin 10mg, atorvastatin 20mg, simvastatin/ezetimibe(vytorin) 10/20mg, simvastatin 40mg, pitavastatin 2mg, fluvastatin XL 80mg, pravastatin 40mg)

Exclusion Criteria

[Exclusion Criteria]
1) Cardiogenic shock
2) Iodinated contrast media administration within the previous 10 days
3) high-intensity statin being used(rosuvastatin 20mg, atorvastatin 40mg or 80mg)
4) Current hemo-dialysis or peritoneal dialysis
5) Thyroid diseases
6) An allergy to the radiocontrast medium
7) Patients who should ban statin
8) Pregnancy
9) Refusal of consent

Study & Design

Study Type
Observational Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Difference of the incidence of cystatin C-based contrast-induced nephropathy within 48 hours between the two groups
Secondary Outcome Measures
NameTimeMethod
Difference of the incidence of cystatin C-based contrast-induced nephropathy within 72 hours between the two groups
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