Acute Heart Failure With Preserved Ejection Fraction - COngestion Discharge Evaluation: Evaluation de la Congestion à la Sortie d'Hospitalisation Pour Insuffisance Cardiaque aiguë à Fraction d'éjection préservée

Status: Recruiting
Location: See location...
Intervention Type: Procedure, Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The AHF-CODE preserved study is a prospective, non-randomized, monocenter study performed in patients with heart failure with preserved ejection fraction admitted for worsening heart failure. The main objective of the AHF-CODE preserved study is to identify congestion markers (clinical, biological and ultrasound) at the end of hospitalization for acute heart failure that are associated with the risk of all cause death or rehospitalization for acute heart failure within 3 months of hospital discharge.

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

• Patients hospitalised for acute heart failure.

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

• Patients considered clinically discharging from hospitalisation for acute heart failure.

• 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
Time Frame
Start Date: 2020-08-29
Estimated Completion Date: 2028-08-29
Participants
Target number of participants: 170
Treatments
Other: Patients hospitalized for acute heart failure
Patients hospitalized for acute heart failure will undergo the following evaluations:~* Clinical examination centered on congestion~* Cardiopulmonary , peritoneal , jugular and renal venous Doppler ultrasounds~* Blood sample retrieved for biological assessment and biobanking~* Telephone interview
Sponsors
Leads: Central Hospital, Nancy, France

This content was sourced from clinicaltrials.gov