Prediction of UA/SOD Ratio as a Biomarker of Oxidative Stress in Atrial Fibrillation
1 other identifier
observational
10,000
1 country
1
Brief Summary
To clarify the predictive effects of uric acid and superoxide dismutase as biomarkers of oxidative stress on atrial fibrillation, and to provide greater value for the diagnosis and prediction of atrial fibrillation. It provides a new idea for the prevention and treatment of atrial fibrillation.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2022
Typical duration 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
January 1, 2022
CompletedFirst Submitted
Initial submission to the registry
September 6, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 31, 2023
CompletedFirst Posted
Study publicly available on registry
November 7, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
April 30, 2024
CompletedNovember 7, 2023
November 1, 2023
1.8 years
September 6, 2023
November 1, 2023
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Uric acid/SOD ratio is associated with atrial fibrillation
Uric acid/SOD ratio is associated with atrial fibrillation
3 years
Study Arms (2)
Atrial Fibrillation cohort
The diagnosis of AF was based on 12-lead electrocardiography (ECG) or 24-hour Holter monitoring, and classification was based on the published 2020 ESC guidelines for the diagnosis and management of AF. The exclusion criteria were as follows: (1) acute heart failure and acute myocardial infarction; (2) severe liver or kidney dysfunction (with aspartate aminotransferase or alanine aminotransferase levels three times higher than normal and estimated glomerular filtration rate \<30 ml/ (min\*1.73 m2)); (3) malignant tumors; and (4) missing data of laboratory indicators at baseline.
Non-atrial Fibrillation cohort
Patients attending the Department of Cardiology to rule out atrial fibrillation.The exclusion criteria were as follows: (1) acute heart failure and acute myocardial infarction; (2) severe liver or kidney dysfunction (with aspartate aminotransferase or alanine aminotransferase levels three times higher than normal and estimated glomerular filtration rate \<30 ml/ (min\*1.73 m2)); (3) malignant tumors; and (4) missing data of laboratory indicators at baseline.
Interventions
ECG of atrial fibrillation last more than 30 seconds.
Eligibility Criteria
This retrospective study enrolled all hospitalized patients from January 2018 to December 2020 at the Department of Cardiology in The First Affiliated Hospital of Shandong First Medical University.
You may not qualify if:
- acute heart failure and acute myocardial infarction;
- severe liver or kidney dysfunction (with aspartate aminotransferase or alanine aminotransferase levels three times higher than normal and estimated glomerular filtration rate \<30 ml/ (min\*1.73 m2));
- malignant tumors;
- missing data of laboratory indicators at baseline.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Yinglong Houlead
Study Sites (1)
Shandong provincal Qianfoshan hospital
Jinan, Shandong, 250014, China
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Hui Tian, PhD
Qianfoshan Hospital
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- professor
Study Record Dates
First Submitted
September 6, 2023
First Posted
November 7, 2023
Study Start
January 1, 2022
Primary Completion
October 31, 2023
Study Completion
April 30, 2024
Last Updated
November 7, 2023
Record last verified: 2023-11
Data Sharing
- IPD Sharing
- Will not share