Prevention of contrast agent - induced acute kidney injury
Conditions
Interventions
Experimental group:Use an automatic hydration therapy device
control group :Routine hydration therapy
Sponsors
The General Hospital of the People's Liberation Army
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: (1) Aged >=18 years; (2) Patients with unstable angina or acute non-ST elevation myocardial infarction (refer to 2019ESC guidelines). (3) Chronic kidney disease (EGFR = 6; (4) Coronary interventional surgery has been performed.
Exclusion criteria
Exclusion criteria: (1) Pregnancy; (2) Acute pulmonary edema within 1 month; (3) Recent use of iodine contrast agent (within 72 hours); (4) To be included in other clinical trials; (5) The use of theophylline, dopamine, mannitol and/or phenoldopam; (6) Patients with end-stage renal disease and routine dialysis; (7) Cardiac shock; (8) Acute left heart failure or acute exacerbation of chronic heart failure within two weeks; (9) Clear allergy to contrast agents or diuretics; (10) There is contraindication of indwelling catheter; (11) The investigator decides that he is not suitable to participate in this study for any other reason.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| CI-AKI%; | — |
Secondary
| Measure | Time frame |
|---|---|
| CI-AKI; | — |
Countries
China
Contacts
Public ContactYunDai Chen
The General Hospital of the People's Liberation Army
Outcome results
None listed