- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05039814
Prediction of Postoperative Acute Kidney Injury in Patients With Acute Type A Aortic Dissection Using Cystatin C
August 1, 2023 updated by: Qilu Hospital of Shandong University
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.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
249
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Shandong
-
Jinan, Shandong, China, 250012
- Qilu Hospital of Shandong University
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Probability Sample
Study Population
patients sufferred acute type A aortic dissection
Description
Inclusion Criteria:
- 18-80 years old
- Acute type A aortic dissection diagnosed by CT angiography
Exclusion Criteria:
- History of chronic kidney disease
- History of cardiovascular operation
- Pregnancy status
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
AKI
patients suffered postoperative acute kidney injury
|
patients suffered postoperative acute kidney injury
|
|
Non-AKI
patients did not suffer postoperative acute kidney injury
|
patients did not suffered postoperative acute kidney injury
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
postoperative acute kidney injury
Time Frame: 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.
|
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.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Xin Zhao, Department of cardiac surgery, Qilu Hospital, Shandong University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
October 1, 2020
Primary Completion (Actual)
June 1, 2021
Study Completion (Actual)
August 15, 2021
Study Registration Dates
First Submitted
September 1, 2021
First Submitted That Met QC Criteria
September 1, 2021
First Posted (Actual)
September 10, 2021
Study Record Updates
Last Update Posted (Actual)
August 3, 2023
Last Update Submitted That Met QC Criteria
August 1, 2023
Last Verified
August 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Cardiovascular Diseases
- Vascular Diseases
- Kidney Diseases
- Urologic Diseases
- Renal Insufficiency
- Aneurysm
- Aortic Diseases
- Female Urogenital Diseases
- Female Urogenital Diseases and Pregnancy Complications
- Urogenital Diseases
- Male Urogenital Diseases
- Dissection, Blood Vessel
- Acute Aortic Syndrome
- Wounds and Injuries
- Acute Kidney Injury
- Aortic Dissection
Other Study ID Numbers
- 81500367
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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