Skip to main content
OpenTrials
Completed

NCT Number: NCT01834833

Consultation at 8 Days to Reduce Hospitalisations in Heart Failure Patient

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

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Hopital Bichat Claude Bernard

Paris, 75018, France

About this study

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)

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Follow-up

Other

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

Primary outcomes

  1. days alive out of hospital 6 months post discharge

    Time frame: 6 months

Secondary outcomes

  1. rehospitalisation rate at 6 months

    Time frame: 6 months

  2. mortality at 3 and 6 months

    Time frame: 3 and 6 months

  3. number of patients receiving beta-blocker at 6 months

    Time frame: 6 months

  4. number of patients receiving a ACEI at 6 months

    Time frame: 6 months

  5. QOL at 6 months

    Time frame: 6 months

  6. autoevaluation of improvement/alteration of the patient state at 6 months

    Time frame: 6 months

  7. number of patients receiving beta-blocker at 3 months

    Time frame: 3 months

  8. number of patients receiving a ACEI at 3 months

    Time frame: 3 months

  9. QOL at 3 months

    Time frame: 3 months

  10. autoevaluation of improvement/alteration of the patient state at 3 months

    Time frame: 3 months

  11. number of patients having an optimal treatment at 6 months

    Time frame: 6 months

  12. number of patients having an optimal treatment at 3 months

    Time frame: 3 months

Sponsors and collaborators

Lead sponsor

Assistance Publique - Hôpitaux de Paris

Other

Registry information

Official study title

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

Acronym: CHIC

Important dates

Study start
2013
Primary completion
2017
Study completion
2017
First posted
Apr 18, 2013
Registry last updated
Oct 23, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.