Clinical Trial Details
— Status: Completed
Administrative data
| NCT number |
NCT04703049 |
| Other study ID # |
YIEAH |
| Secondary ID |
|
| Status |
Completed |
| Phase |
|
| First received |
|
| Last updated |
|
| Start date |
July 10, 2017 |
| Est. completion date |
November 30, 2017 |
Study information
| Verified date |
August 2021 |
| Source |
Bursa Postgraduate Hospital |
| Contact |
n/a |
| Is FDA regulated |
No |
| Health authority |
|
| Study type |
Observational
|
Clinical Trial Summary
In our study, we aimed to investigate how whole blood viscosity (WBV) affects the development
of contrast-induced nephropathy (CIN) in patients undergoing percutaneous coronary
intervention (PCI).
Description:
In our study, 500 patients who applied to the cardiology clinic and underwent PCI for
elective procedure, ST segment elevation myocardial infarction (STEMI), and non-STEMI were
prospectively included. Before the procedure, we calculated WBV using the formula [(0.12 ×
hematocrit) + (0.17 × (total protein - 2.07)]. We defined CIN as the absolute (≥0.5 mg/dl) or
relative increase (≥25%) in serum creatinine 48-72 h after exposure to a contrast agent
compared with baseline serum creatinine values.