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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04473144
Other study ID # MED-MDB_20-257
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date August 1, 2020
Est. completion date August 31, 2021

Study information

Verified date July 2020
Source Ajou University School of Medicine
Contact ji young yoo, assistant professor
Phone 821056902104
Email springbear@nate.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Acute kidney injury (AKI) is a frequent complication after cardiac surgery. AKI has been reported as 7-40% depending on the type of surgery, and is known to increase to about 50% when there are risk factors. Cardiac surgery-associated AKI (CSA-AKI) requires cardiac replacement therapy in 1-5% of patients and increases mortality to 1,4%, but the treatment is still unknown. Therefore prevention of occurrence is very important.

Known factors related to the development of CSA-AKI include hemodynamic, inflammatory, metabolic, and nephrotoxic factors, and since there is a close connection between hypotension due to deterioration of cardiac function, preventive measures to prevent hypotension in juicing It is only possible.

To date, strategies to protect kidneys with drugs are very limited. Urinary trypsin inhibitor, ulistine, has anti-inflammatory and antioxidant effects, so it has been reported to protect against renal ischemia/reperfusion injury. Various studies have been attempted to prevent CSA-AKI, but most of them are inflammatory reactions during surgery. It was performed only for surgery with extracorporeal circulation that causes severely.

Therefore, this study would like to verify the effectiveness of ulistine's medicine in the prevention of CSA-AKI in patients undergoing coronary artery bypass surgery without extracorporeal circulation.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 500
Est. completion date August 31, 2021
Est. primary completion date July 1, 2021
Accepts healthy volunteers No
Gender All
Age group 19 Years and older
Eligibility Inclusion Criteria:

- From January 2015 to June 2020, a retrospective study will be conducted on patients undergoing extracorporeal circulatory coronary artery bypass surgery at Ajou University Hospital.

Exclusion Criteria:

- Patients who were undergoing renal replacement therapy prior to surgery due to end-stage renal failure are excluded from the study.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Ulinastatin
In the Ulistine administration group, 300,000 KIU was mixed with 100 mL physiological saline and administered over 15 minutes after induction of anesthesia.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Ajou University School of Medicine

Outcome

Type Measure Description Time frame Safety issue
Primary The incidence of acute kidney injury Cr = 0.3 mg/dl within 48 hours after surgery, 1.5 times higher preoperative value within 7 days, urine volume <0.5 ml/kg for 6 hours after surgery 7 days after operation
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