Transient Ischemic Attack (TIA) Clinical Trials

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Hospital-acquired Pneumonia After Cardiovascular Surgery (CS): the Prediction and Assessment of Long-term Cardiovascular and Pulmonary Outcomes With Artificial Intelligence (AI) - (PNEUMONIA-CS-AI)

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Observational
SUMMARY

This multicenter, prospective, observational study aims to address two primary objectives. The first objective is to demonstrate that hospital-acquired pneumonia (nosocomial pneumonia) following cardiac surgery can be predicted using artificial intelligence (AI), and to develop a personalized risk calculator for its development. The second objective is to demonstrate that hospital-acquired pneumonia can serve as a risk factor for a 1-year composite cardiovascular and pulmonary outcome after cardiac surgery, and to develop a personalized risk calculator for this composite outcome. The composite outcome will include the occurrence of any of the following events: * Respiratory death * Hospitalization for respiratory diseases * Development of oxygen dependence * New-onset asthma, COPD, or interstitial lung disease * Initiation or intensification of bronchodilator or corticosteroid therapy * Cardiovascular death * Acute myocardial infarction * Unstable angina * Myocardial revascularization * Acute ischemic stroke * Transient ischemic attack * Acute heart failure * Hospitalization for decompensated heart failure * New-onset atrial fibrillation or ventricular tachycardia * Initiation or intensification of antiarrhythmic therapy Both objectives will be addressed using artificial intelligence technologies applied during the data analysis phase. This is a non-interventional study. Patient evaluation and treatment are conducted in strict accordance with approved standards of medical care for the respective conditions. No experimental or unregistered (not approved for use in the Russian Federation) medical or diagnostic procedures will be performed during this study.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Age ≥ 18 years;

• Cardiac and/or vascular surgical intervention during the current hospitalization;

• Signed informed consent from the patient for the use of their anonymized data for scientific purposes.

Locations
Other Locations
Russian Federation
Cardiology Research Institute, Tomsk National Research Medical Center, Russian Academy of Sciences, Tomsk, Russia
RECRUITING
Tomsk
Contact Information
Primary
Alla A. Boshchenko, MD, PhD, DSc
bosh@cardio-tomsk.ru
+ 7 (3822)-909055
Backup
Tatiana P. Kalashnikova, MD, PhD
kalashnikova-t@mail.ru
+7 913 814 1664
Time Frame
Start Date: 2026-07-29
Estimated Completion Date: 2028-09-30
Participants
Target number of participants: 700
Treatments
Patients after cardiovascular surgery
Patients of 18 years and older, after cardiac and/or vascular surgical intervention during the current hospitalization, who signed informed consent for the use of their anonymized data for scientific purposes
Sponsors
Leads: Tomsk National Research Medical Center of the Russian Academy of Sciences
Collaborators: National Research Tomsk State University, Research Institute for Complex Problems of Cardiovascular Diseases, Russia

This content was sourced from clinicaltrials.gov