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Clinical Trials in France / NCT05089149
Recruiting Not applicable

Chronic Heart Failure - COngestion eValuation

NCT05089149 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2021-12-14
Last updated
2023-06-05

Condition(s) studied

Chronic Heart Failure

Investigational drug(s) / intervention(s)

Clinical examination centered on congestionCardiac, pulmonary, peritoneal, jugular, renal Doppler ultrasounds and liver elastographyBlood sample retrieved for biological assessment and biobankingTelephone follow-upKansas City Cardiomyopathy Questionnaire (KCCQ)

Clinical examination centered on congestion: Clinical examination (including the EVEREST, ASCEND and Ambrosy scores) centered on congestion will be performed during day hospitalization or consultation

Cardiac, pulmonary, peritoneal, jugular, renal Doppler ultrasounds and liver elastography: Cardiac, pulmonary, peritoneal, jugular and renal Doppler ultrasounds will be performed during day hospitalization or consultation/ peritoneal, jugular and renal Doppler ultrasounds and liver elastography are optional

Blood sample retrieved for biological assessment and biobanking: Blood sample retrieved for biological assessment and biobanking will be performed during day hospitalization or consultation

Telephone follow-up: Telephone follow-up will be performed 3, 12 and 24 months after visit (during day hospitalization or consultation)

Kansas City Cardiomyopathy Questionnaire (KCCQ): Questionnaire centered on patient's quality of life at discharge and 3, 12 and 24 months after discharge

Study summary

Heart failure (HF) is a significant cause of death and the leading cause of hospitalization in patients over 65 years of age. Congestion is the main source of symptoms and the leading cause of hospitalization for HF. Furthermore, congestive signs identified in asymptomatic patients are associated with the risk of developing symptomatic HF. The literature supports a multi-modality / integrative evaluation of congestion, combining clinical examination, laboratory results and ultrasound evaluation.

The main objective of the CHF-COV study is to identify congestion markers (clinical, biological and ultrasound) quantified during a consultation or day hospitalization for the monitoring of chronic HF that are associated with the risk of all-cause death or hospitalization for acute HF within 24 months after day hospitalization.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients with chronic acute heart failure admitted in hospital for scheduled day hospitalization or consultation * Age ≥18 years * Patients having received complete information regarding the study design and having signed their informed consent form. * Patient affiliated to or beneficiary of a social security scheme. Exclusion Criteria: * Comorbidity for which the life expectancy is ≤ 3 months * Dialysis patient (peritoneal dialysis or hemodialysis) or patients with glomerular filtration rate \<15 ml/min/m2 at inclusion. * History of lobectomy or pneumonectomy lung surgery * Severe pulmonary or pleural pathology preventing reliable acquisition of lung ultrasound images: severe emphysema, chronic pleurisy, pulmonary fibrosis, etc. * Pregnant woman, parturient or nursing mother * Adult person subject to a legal protection measure (guardianship, curatorship, safeguard of justice) * Adult person who is unable to give consent * Person deprived of liberty by a judicial or administrative decision, * Person subject to psychiatric care pursuant to Articles L. 3212-1 and L. 3213-1 of the Public Health Code.

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
CHRU de Nancy Vandœuvre-lès-Nancy France Recruiting
CHRU de Nancy Vandœuvre-lès-Nancy France Not Yet Recruiting

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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 NCT05089149 on ClinicalTrials.gov ↗ ← All trials in France