Effects of Intraoperative Hemoperfusion on Acute Kidney Injury After Aortic Dissection
NCT ID: NCT05331495
Last Updated: 2022-04-15
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
206 participants
INTERVENTIONAL
2022-04-20
2024-12-31
Brief Summary
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Detailed Description
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The general process of this study is that the patients with AAD treated in our hospital who needed surgical treatment were randomly divided into two groups according to the inclusion and exclusion criteria. The control group was treated with intraoperative CPB and DHCA, and the experimental group was treated with hemoperfusion simultaneously with CPB and DHCA. By detecting the expression level of CIRP in the postoperative serum and the incidence of AKI within 7 days after the operation, the prognosis difference between the two groups was analyzed.
Follow-up content: Collect preoperative clinical data, that is, general information of patients: hospital number, name, gender, age, BMI, smoking history, history of hypertension, diabetes, myocardial infarction and angina pectoris, history of chronic obstructive pulmonary disease, peripheral vascular disease, and brain vascular accident, cardiac function classification, cardiac ultrasonography EF value, preoperative creatinine level, eGFR, cystatin C level, hemoglobin Hct, preoperative CTA results whether the lesion involved renal artery and whether preoperative poor organ perfusion performance. The main evaluation index of postoperative follow-up was whether AKI occurred within 7 days after surgery. The diagnostic criteria for AKI were based on the KDIGO diagnostic criteria. The secondary evaluation criteria were the expression level of serum CIRP 24 hours after surgery, and the changes in the expression level of serum inflammatory factors within 7 days after surgery, and the postoperative survival rate, ventilator assistance time, ICU hospitalization time, postoperative hospitalization time, infection and SOFA score.
The criteria for the termination or withdrawal of the study subjects were that the family members of the patients gave up the follow-up treatment due to personal reasons (economic reasons, etc.), or coronary artery bypass grafting was required due to lesions during the operation, or serious complications such as poor cardiac resuscitation and difficulty in hemostasis occurred or ECMO assistance.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Hemoperfusion and CPB and DHCA surgery
The experimental group was treated with hemoperfusion simultaneously with CPB and DHCA.
Intraoperative Hemoperfusion
During the operation, the hemoperfusion device and the membrane oxygenator of the extracorporeal circulation device were operated in parallel.
traditional CPB and DHCA surgery
The control group was treated with intraoperative CPB and DHCA surgery.
No interventions assigned to this group
Interventions
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Intraoperative Hemoperfusion
During the operation, the hemoperfusion device and the membrane oxygenator of the extracorporeal circulation device were operated in parallel.
Eligibility Criteria
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Inclusion Criteria
* Patients had aortic dissection type A with onset within 7 days.
Exclusion Criteria
* Past history of renal insufficiency;
* Difficulty in hemostasis during operation due to taking anticoagulant and antiplatelet drugs for various reasons before operation, and the CPB time exceeds 4 hours;
* Severe organ perfusion before surgery, such as lower extremity ischemia or preoperative coma;
* BMI\>40 Kg/m\^2 or pregnancy status.
18 Years
75 Years
ALL
No
Sponsors
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First Affiliated Hospital Xi'an Jiaotong University
OTHER
Responsible Party
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Principal Investigators
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Xinglong Zheng, PhD
Role: STUDY_CHAIR
First Affiliated Hospital of Xian Jiaotong University
Locations
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First Affiliated Hospital of Xian Jiaotong University
Xi'an, Shaanxi, China
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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XJTU1AF2021CRF-029
Identifier Type: -
Identifier Source: org_study_id
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