Actively Recruiting
Application of CLCVP Technique in Early Intervention of CSA-AKI
Led by Nanjing First Hospital, Nanjing Medical University · Updated on 2025-05-30
200
Participants Needed
1
Research Sites
139 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this clinical trial is to learn about in postoperative acute kidney injury in cardiac surgery. The main questions it aims to answer are: 1. Controlled low central venous pressure (CLCVP) technique can reduce the occurrence of cardiac surgery-associated acute kidney injury (CSA-AKI) by reducing venous congestion and increasing renal perfusion pressure. 2. CLCVP technique does not increase the risk of postoperative cognitive dysfunction (POCD) during cardiac surgery. Participants who are assigned to the intervention group will receive CLCVP technique. Specific methods are as follows: First,20min after the end of cardiopulmonary bypass, on the basis of ensuring that the mean arterial pressure (MAP) ≥ 60mmHg, the patients will accept dorsal elevated position. After that, if the patient's central venous pressure (CVP) is less than 10mmHg, nitroglycerin will be pumped at 0.2ug/ (kg \* min). If the patient's CVP is still greater than or equal 10mmHg, we increase the dose by 0.2ug/ (kg \* min) and pump again for 5min, and the like. Until the patient's CVP is less than 10mmHg or the dose of nitroglycerin increases to 1ug/ (kg \* min), the current dose is maintained until the end of surgery. If participants are assigned to the control group, no intervention measures will be taken. The researchers will compare the intervention group with the control group to see the occurrence of CSA-AKI and POCD after cardiac surgery.
CONDITIONS
Official Title
Application of CLCVP Technique in Early Intervention of CSA-AKI
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged 18 years and older who underwent cardiac surgery such as coronary artery bypass grafting, heart valve surgery, heart transplant, or surgical removal of intracardiac myxoma
You will not qualify if you...
- Pre-existing renal insufficiency defined by abnormal preoperative serum creatinine 133 bcmol/L or diagnosis of renal insufficiency within 6 months before surgery
- Dialysis dependence within 60 days before surgery
- Off-pump heart surgery
- Prior kidney transplantation
- Pregnancy
- Current treatment with nitroglycerin
AI-Screening
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Trial Site Locations
Total: 1 location
1
Nanjing First Hospital
Nanjing, Jiangsu, China, 210012
Actively Recruiting
Research Team
Y
Yali Ge, Doctor
CONTACT
L
Lanxin Hu, BS
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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