Évaluation de la Congestion en Ambulatoire Chez Les Patients Atteints d'Insuffisance Cardiaque Chronique à Fraction d'éjection préservée. CHF-COV Preserved (Chronic Heart Failure With Preserved Ejection Fraction - COngestion eValuation)

Status: Recruiting
Location: See location...
Intervention Type: Procedure, Behavioral, Other
Study Type: Interventional
Study Phase: Not Applicable
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 Preserved study is to identify congestion markers (clinical, biological and ultrasound) quantified during a consultation or day hospitalization for the monitoring of chronic HF with preserved left ventricular ejection fraction that are associated with the risk of all-cause death, hospitalization for acute HF or IV diuretics injection in a day hospital.

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

• Patients with chronic acute heart failure with preserved ejection fraction admitted in hospital for scheduled day hospitalization or consultation

• Patient with preserved left ventricular ejection fraction (≥50%).

• 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

Locations
Other Locations
France
CHRU de Nancy
RECRUITING
Vandœuvre-lès-nancy
Contact Information
Primary
Nicolas GIRERD, MD, PhD
n.girerd@chru-nancy.fr
+ 33 3 83 15 73 22
Backup
Sanae BOUALI
s.bouali@chru-nancy.fr
+ 33 3 83 15 73 22
Time Frame
Start Date: 2022-08-10
Estimated Completion Date: 2029-06-10
Participants
Target number of participants: 200
Treatments
Experimental: Patients with chronic HFpEF coming for scheduled day hospitalization or consultation
* Clinical examination focusing on congestion~* Cardiac, pulmonary, peritoneal, jugular and renal venous Doppler ultrasounds~* Blood sample retrieved for biological assessment and biobanking~* Telephone follow-up
Sponsors
Leads: Central Hospital, Nancy, France

This content was sourced from clinicaltrials.gov