Viewing Study NCT06544538



Ignite Creation Date: 2024-10-26 @ 3:37 PM
Last Modification Date: 2024-10-26 @ 3:37 PM
Study NCT ID: NCT06544538
Status: COMPLETED
Last Update Posted: None
First Post: 2024-07-27

Brief Title: Acute Kidney Injury After Cardiac Arrest
Sponsor: None
Organization: None

Study Overview

Official Title: Causes and Clinical Outcomes of Acute Kidney Injury After Cardiac Arrest A Retrospective Cohort Study
Status: COMPLETED
Status Verified Date: 2024-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The development of AKI Acute Kidney Injury after cardiac arrest is a common factor associated with mortality In this study we aimed to evaluate the factors that increase the risk of developing AKI after cardiac arrest

For the study patients were evaluated for the incidence of acute kidney injury AKI factors that increase the risk of AKI and the impact of AKI on mortality In this process demographic data comorbidities hemodynamic data laboratory data clinical symptoms and findings recorded in the electronic decision support system were recorded and analyzed
Detailed Description: This retrospective study was performed on patients hospitalized in intensive care units after cardiac arrest between 2013 and 2022 Patients who met the inclusion criteria were included in the study Urea creatinine values and whether AKI was diagnosed or not were obtained from the data registry system Statistical evaluation was performed using univariate binary logistic regression analysis

Demographic data location of cardiac arrest in-hospital out-of-hospital and duration of CPR were recorded In addition the causes of cardiac arrest HRMAP heart rateaverage arterial pressure ratio and whether VSP vasopressor or INO inotropic medication was needed were recorded

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None