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Cohort of Heart Failure Patients

Lyon and Rhône Alpes Auvergne Registry of Congestive Heart Failure

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03422991
Acronym
LOOP-HF
Enrollment
150
Registered
2018-02-06
Start date
2017-12-15
Completion date
2024-01-16
Last updated
2024-11-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Congestive Heart Failure

Keywords

Heart Failure, Heart Diseases, Cardiovascular Diseases, Vascular Diseases, Cohort

Brief summary

This is a prospective cohort study of patients with Heart Failure with an eighteen-month follow-up aimed to collect all demographic, clinical, biological and para-clinical data to study population characteristics, assess prognosis markers and occurrence of HF treatment side effects. Congestive Heart failure is a frequent pathology and its prevalence increases with age. Its prognosis stays pejorative despite years of major therapeutical progress. In recent trials, all-cause mortality rates at 1-year reach up to 20% and 50% at 5 years. Medical care of congestive heart failure is based on precise international recommendations. The association of Beta-Blockers, renin-angiotensin system blockers, mineralocorticoid receptor antagonists, represent the basis of the pharmacological treatment. Cardiac resynchronization treatment and implantable cardioverter-defibrillator are additional efficient treatments that reduce events in appropriately selected patients. Despite these improvements, the prognostic of congestive heart failure in registers is worse than those observed in randomized trials. This can be explained by differences in congestive heart failure patient populations and/or by a less rigorous medical care where treatments are not optimized. The evaluation of medical care in congestive heart failure is today of utmost importance. Integrating new pharmacological molecules, medical devices and the application of new recommendations have major interest for documentation and practical changes. The main objective of this cohort will be to evaluate the evolution of the 12-month quality of life score of a HF patient and the characteristics and treatments associated with it.

Interventions

OTHERBlood sampling and Quality of life questionnaire.

Blood sampling and Quality of life questionnaire.

Sponsors

Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients with congestive heart failure confirmed during * Hospitalization for cardiac decompensation * A medical follow-up for stable congestive heart failure with at least one cardiac decompensation event * NT-proBNP \> 500 ng/l in the month before Baseline (or BNP \> 150 ng/l) * NYHA ≥ 2 * Aged over 18 * Signature of the informed consent

Exclusion criteria

* Life expectancy shorter than a month * Patients on long term assistance or with heart transplant * Impossibility to give patients clear information * Loss of autonomy, dementia, major dependence * Patients without health coverage * Patient with no legal protection * Pregnant woman

Design outcomes

Primary

MeasureTime frameDescription
Change from Baseline Quality of life questionnaire : EuroQol (EQ-5D) at 12 months12 monthsMeasurement of quality of life of patients with heart failure: patient will answer to this questionnaire (Mobility, Autonomy of the person, Current activities, Pain ,Anxiéty/Depression) ) at baseline and at 12th month visit. The evolution between these two scores will be analysed .

Secondary

MeasureTime frameDescription
NT-proBNP18 monthsMeasure of NT-proBNP will be done at 18th month in order to correlate the effect of low blood pression and renal function decreasing on NT-proBNP variability
number of death (all-cause)18 months
number of all cardiovascular cause death18 months
number all unscheduled hospitalization for heart failure18 months
number of stroke18 months
nonfatal myocardial infarction18 months
Renal function : glomerular filtration rateBaselineAssessing the renal function evolution of patients with heart failure the glomerular filtration rate will be calculated according to CKD-EPI (Chronic Kidney Disease - Epidemiology Collaboration) formula.
symptomatic hypotension18 months
number of dialysis18 months
number ventricular arrhythmias18 months(ventricular tachycardia and ventricular fibrillation)
Heart failure stage will be assessed thanks to the New York Heart Association (NYHA) classificationBaseline, 6, 12 and 18 months
Cardiac functionBaseline and 12 monthsCardiac function will be evaluated on Echography Trans Thoracic at baseline and at the 12 months visit. * Left Ventricular Ejection Fraction * levitation pressure filling (yes/No) * Right ventricular dysfunction (yes/no) * pulmonary artery systolic pressure (mmHg) * right atrial pressure
cardiac assistance or heart transplantation18 months

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026