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Starting soon Observational

Delirium and Heart Failure

NCT07302737 · tracked via the Priya Life Science Egypt tracker
Phase
Observational
Started
2026-01-20
Last updated
2025-12-24

Condition(s) studied

Heart FailureDelirium Confusional State

Investigational drug(s) / intervention(s)

Comprehensive Geriatric Assessmentthe Confusion Assessment Method (CAM test) or CAM-ICUDelirium Rating Scale - Revised-98blood biomarkers

Comprehensive Geriatric Assessment: multidimensional assessment of cognition, physical, function, mood, social status of the participants

the Confusion Assessment Method (CAM test) or CAM-ICU: standardized tool designed to quickly and accurately diagnose delirium by assessing four key features: acute mental change, inattention, and either disorganized thinking or altered consciousness. The original CAM is used for communicative patients on general wards, relying on conversation, while the CAM-ICU is adapted for critically ill, often non-verbal patients in the ICU, using non-verbal tasks and sedation scales. By providing a rapid, reliable method for identifying this often-missed condition, both tools trigger crucial medical interventions, helping to mitigate delirium's serious risks, including longer hospital stays, long-term cognitive decline, and increased mortality.

Delirium Rating Scale - Revised-98: The Delirium Rating Scale-Revised-98 (DRS-R-98) is a standardized, expert-rated clinical tool designed specifically to measure the severity of delirium and help distinguish it from other psychiatric disorders, such as dementia, depression, and schizophrenia. Unlike the CAM/CAM-ICU, which provides a simple "yes/no" diagnosis, the DRS-R-98 quantifies how severe a patient's delirium is at a given point in time and tracks changes in that severity over the course of the illness

blood biomarkers: complete blood count(to obtain systemic inflammatory index) ,triglyceride (TG) and glucose, Liver and kidney function tests and serum electrolytes level

Study summary

Biomarkers such as Systemic Immune-Inflammation Index (SII) and TG/Glucose Ratio (TyG) have shown promise in predicting delirium, reflecting the roles of inflammation and metabolic disturbances in its pathophysiology. This study aims to compare the predictive value of SII and the TyG ratio among other chemical and physiological biomarkers for diagnosing delirium and detecting its severity in older adults with heart failure. These biomarkers reflect different pathophysiological pathways implicated in delirium, including inflammation, cardiovascular stress, and metabolic dysfunction. By evaluating their individual and combined predictive abilities, this research seeks to identify potential tools for early identification of patients at high risk for delirium

Eligibility

Sex
ALL
Min age
60 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: Heart failure stage C Exclusion Criteria: 1. cognitive impairment 2. Major Neurological Conditions: (e.g., stroke, traumatic brain injury). 3. Hematological diseases that affect platelet, neutrophil, and lymphocyte counts. 4. Cardiogenic Shock 5. Sepsis 6. Ongoing Treatment with Immunosuppressants, or corticosteroids

Primary outcome measure(s)

  • the sensitivity and specificity of different biomarkers of delirium in heart failure older patient — Within 24 hours of hospital admission
    assess sensitivity and specificity of the systemic inflammatory index (SII), Rate Pressure Product (RPP), and TG/glucose ratio in predicting delirium

Trial sites (1)

FacilityCityRegionStatus
Ain Shams University hospitals Cairo Egypt
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07302737 on ClinicalTrials.gov ↗ ← All trials in Egypt