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Consultation at 8 Days to Reduce Hospitalisations in Heart Failure Patient

Consultation at 8 Days to Reduce Hospitalisations in Heart Failure Patient.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01834833
Acronym
CHIC
Enrollment
326
Registered
2013-04-18
Start date
2013-05-31
Completion date
2017-07-31
Last updated
2018-10-23

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

Conditions

Acute Heart Failure

Keywords

Acute heart failure; rehospitalisation; education; follow-up

Brief summary

Evaluate the benefit of systematic appointment with a cardiologist a week after hospitalisation for acute heart failure. Randomised, endpoint: number of day alive out of hospital during 6 months

Detailed description

Background: the risk for rehospitalisation is very high after hospitalisation for acute heart failure. Aim: evaluate the benefit of a consultation with a cardiologist, including echocardiography and education of the patient, between 7 and 15 days after discharge, in high risk patients, identified with BNP or incomplete therapy. Parallel randomised study. The main endpoint is the number of day alive out of hospital during the 6 months post discharge; statistics intention to treat comparison of the number of days alive out of hospital in the group with consultation compared with the group without consultation. Recruitment 3 years and 4 months, follow-up 6 months. Patients included have been hospitalised in hospital BICHAT 75018 Paris, France. Financing is by the ministry of health (PHRQHOS)

Interventions

OTHERFollow-up

Evaluation by a cardiologist using echocardiography, completed by education of the patient if necessary

Sponsors

Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

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

Inclusion criteria

Criteria of inclusion : * Patient with decompensated heart failure hospitalized in the hospital BICHAT, * For whom is planned a return at home, * Valid (being able to return for a consultation to the hospital) * Having Nt-ProBNP of exit ≥ 3500 ng /l and/or a non optimized treatment of exit - according to the doctor who has it the responsibility, * Having signed the consent form by participation in the study. Criteria of not inclusion : * Age \< 18 years, * Not membership in a national insurance scheme or in the Universal Health * Coverage (CMU)(FREE UNIVERSAL HEALTH CARE)(A patient benefiting from the Medical aid of the State (AME) cannot be included) * Participation to another protocol of research, * Not being reachable by telephone in 6 months.

Design outcomes

Primary

MeasureTime frame
days alive out of hospital 6 months post discharge6 months

Secondary

MeasureTime frame
mortality at 3 and 6 months3 and 6 months
number of patients receiving beta-blocker at 6 months6 months
number of patients receiving a ACEI at 6 months6 months
QOL at 6 months6 months
autoevaluation of improvement/alteration of the patient state at 6 months6 months
rehospitalisation rate at 6 months6 months
number of patients receiving a ACEI at 3 months3 months
QOL at 3 months3 months
autoevaluation of improvement/alteration of the patient state at 3 months3 months
number of patients having an optimal treatment at 6 months6 months
number of patients having an optimal treatment at 3 months3 months
number of patients receiving beta-blocker at 3 months3 months

Countries

France

Outcome results

None listed

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