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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04984928
Other study ID # RECHMPL21_0488
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date September 20, 2021
Est. completion date December 30, 2022

Study information

Verified date April 2022
Source University Hospital, Montpellier
Contact Grégoire Mercier, PU PH
Phone 4 67 33 91 09
Email g-mercier@chu-montpellier.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Heart failure (HF) is a frequent, serious, and costly chronic disease: it leads to 150,000 hospitalizations each year in France at a cost of 525 million Euros. It is estimated that 20-40% of these hospitalizations are preventable by known interventions: home telemonitoring, care coordination, therapeutic intensification and therapeutic education. But these interventions only work if patients at high risk of rehospitalization are targeted to individualize management. In these patients, the risk of rehospitalization depends on clinical, biological, socioeconomic, care pathway, and location-related data. Existing predictive tools perform poorly due to three important limitations: non-use of unstructured clinical data, lack of integration of multimodal data, and weakness of the algorithmic approach. The objective is to design and validate a predictive algorithm for the risk of rehospitalization in heart failure patients, using multiple data sources


Recruitment information / eligibility

Status Recruiting
Enrollment 1500
Est. completion date December 30, 2022
Est. primary completion date December 1, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion criteria: - All consecutive adults - Admitted to Montpellier University Hospital in 2017-2020 - For heart failure Exclusion criteria: - age < 18 years

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Uh Montpellier Montpellier

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Montpellier

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary 30 days all cause readmission rate 30 days all cause readmission rate day 30
Secondary 90 days all cause readmission rate 90 days all cause readmission rate day 90
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