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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02763670
Other study ID # 2013.838
Secondary ID
Status Completed
Phase N/A
First received May 3, 2016
Last updated February 12, 2018
Start date September 2015
Est. completion date December 2017

Study information

Verified date February 2018
Source Hospices Civils de Lyon
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The heart failure is a chronic pathology with prevalence from 2 to 3% of general population, a death rate of 50% at 6 months for patients with stage IV, and a probability of death or hospitalization or emergency consultation of 40% at 3 years. The care of patients is heterogeneous, especially in light of the organization of therapeutic education offered to patients and patient monitoring modalities.

The aim of this study is to investigate the management strategies for patients with chronic heart failure stage III or IV NYHA, and heart failure patients with stage II NYHA with previous hospitalization for heart failure.

This is a longitudinal observational multicenter study comparing a management strategy including patient education and monitoring as part of a hospital dedicated organization and an organization of care as usually done in France.

The primary endpoint was a composite endpoint of morbidity and mortality involving deaths, unplanned readmissions and emergency visits for heart failure.

The expected number of patients is 720 patients (360 per strategy). The follow-up duration of 24 months.


Recruitment information / eligibility

Status Completed
Enrollment 186
Est. completion date December 2017
Est. primary completion date December 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria:

- Chronic heart failure patient with left ventricular ejection fraction (LVEF) defined by an impaired LVEF less than or equal to 40%.

- Heart failure stage III or IV NYHA, or heart failure patients with stage II NYHA with previous hospitalization for heart failure.

- Patient who has received a written or oral information of the study

- Patient affiliated with French health Insurance

Exclusion Criteria:

- Patient refusal to participate in the study

- Progressive neoplastic pathology.

- Patient with impaired cognitive functions known.

- Patient subject to a measure of socio-legal protection.

- Heart failure secondary to curable causes (an arrhythmia, valvular dysfunction, myocardial infarction, bypass surgery scheduled, aortic stenosis, breaking rope…)

- Dyspnea pulmonary origin: pulmonary arterial hypertension pre-capillary origin catheterization, defined by a Pcap =15 mmHg.

- Patient who underwent ventricular mechanical assistance.

- Patient with acute breathlessness is explained by: a severe lung infection (CPT <60% of predicted, ventricular ejection fraction <60% predicted) or pulmonary embolism or respiratory failure with ambient air PaO2 (arterial oxygen pressure) below 60 mmHg or oxygen therapy.

- Dialysis patient

Study Design


Related Conditions & MeSH terms


Intervention

Other:
PRETICARD patient care management
A standardized and specialized network to take care of the severe cardiac insufficiency: An initial assessment and consultations with health professionals specialized in severe cardiac insufficiency during the hospitalization for cardiac insufficiency At 1 months, consultations and acts realized by health professionals specialized (one hospital day care) At 2 months, a therapeutic education program for heart failure patients, approved by the Rhône-Alpes regional public health authorities (week hospital: two days and one night). At 6 and 18 months, one cardiology consultation At 12 and 24 months, consultations and acts realized by health professionals specialized (one hospital day care)
"As usual " patient care management
Conventional management of heart failure patients is defined in the guide HAS ("Haute Autorité de Santé") care course. Patient follow-up, however, is defined by the patient's physician and / or cardiologist at the waning of his hospitalization, according to the usual practice for patients with stage II, III or IV NYHA. According to these recommendations, the patient should see his cardiologist at least once a year. Usual practices are: An initial assessment and consultations with health professionals specialized in severe cardiac insufficiency during the hospitalization for cardiac insufficiency At 12 months, a cardiologic consultation. For the study, three evaluation points are programmed: two by phone at 6 and 18 months, two by a consultation at 24 months. This interview aimed to evaluate the number of hospitalization, consultations and acts realized by health professionals specialized (the information in the logbook).

Locations

Country Name City State
France Hospices Civils de Lyon Bron

Sponsors (1)

Lead Sponsor Collaborator
Hospices Civils de Lyon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Composite endpoint combining the proportion of patients who died, the proportion of hospitalization for heart failure as well as the proportion of emergency visits for heart failure. 12 months
Secondary Unplanned re hospitalization rate or emergency consultations for cardiac insufficiency. At 6, 18 and 24 months
Secondary Quality of life. MINNESOTA Questionnaire. 12 months
Secondary Satisfaction. Semi-structured interviews. 3 months
Secondary Cost of medical care Identification of expenditure:
Hospitalizations
Consultations (inpatient and outpatient)
Biology and imaging
Medical transport
24 months
See also
  Status Clinical Trial Phase
Recruiting NCT03062241 - Ablation of Atrial Fibrillation in Heart Failure Patients N/A