Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05855954

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

Nanjing First Hospital

Nanjing, Jiangsu, China, 210012

Actively Recruiting

Loading map...

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

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here