Prediction of Postoperative Acute Kidney Injury in Patients With Acute Type A Aortic Dissection Using Cystatin C
1 other identifier
observational
249
1 country
1
Brief Summary
The research aimed to predict postoperative acute kidney injury in patients with acute type A aortic dissection preliminarily by exploring the correlation of preoperative cystatin C level and incidence of postoperative acute kidney injury and combining with relevant risk factors.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Oct 2020
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 1, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
August 15, 2021
CompletedFirst Submitted
Initial submission to the registry
September 1, 2021
CompletedFirst Posted
Study publicly available on registry
September 10, 2021
CompletedAugust 3, 2023
August 1, 2021
8 months
September 1, 2021
August 1, 2023
Conditions
Outcome Measures
Primary Outcomes (1)
postoperative acute kidney injury
YES; NO
From date of operation until the date of acute kidney injury or date of death from any cause, whichever came first, assessed up to 30 days.
Study Arms (2)
AKI
patients suffered postoperative acute kidney injury
Non-AKI
patients did not suffer postoperative acute kidney injury
Interventions
patients did not suffered postoperative acute kidney injury
Eligibility Criteria
patients sufferred acute type A aortic dissection
You may qualify if:
- years old
- Acute type A aortic dissection diagnosed by CT angiography
You may not qualify if:
- History of chronic kidney disease
- History of cardiovascular operation
- Pregnancy status
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Qilu Hospital of Shandong University
Jinan, Shandong, 250012, China
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Xin Zhao
Department of cardiac surgery, Qilu Hospital, Shandong University
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 1, 2021
First Posted
September 10, 2021
Study Start
October 1, 2020
Primary Completion
June 1, 2021
Study Completion
August 15, 2021
Last Updated
August 3, 2023
Record last verified: 2021-08