- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04845126
Outcomes of Patients With Heart Failure Hospitalized in an Internal Medicine Unit
Outcomes of Patients With Heart Failure Hospitalized in an Internal Medicine Unit - a Four Years Follow-up Study
In 2018, the investigators evaluated the treatment of 236 patients with heart failure (with preserved or reduced ejection fraction) before and after hospitalization in our internal medicine unit (from 2016 to 2017).
The investigators showed that patients, mainly elderly women with comorbidities, often had suboptimal heart failure treatment without an identified cause. The investigators tried, whenever possible, to optimize treatment before hospital discharge.
Our objective is now to analyze the 4-year outcome of these patients, including re-hospitalization for heart failure or death.
Study Overview
Status
Conditions
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Montpellier, France, 34295
- University hospital of Montpellier
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion criteria:
- Patients hospitalized in our Internal Medecine unit for acute heart failure or for another cause but with known chronic heart Failure
Exclusion criteria:
- Hemodilaysis, end stage kidney disease, heart failure cause by anuria, heart transplantation
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
re-hospitalization for heart failure or death failure assessed by spirometry
Time Frame: 1 day
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re-hospitalization for heart failure or death (yes or no) (composite outcome)
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1 day
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
time to re-hospitalization
Time Frame: 1 day
|
time to re-hospitalization
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1 day
|
time to death
Time Frame: 1 day
|
time to death
|
1 day
|
cause of hospitalization
Time Frame: 1 day
|
cause of hospitalization
|
1 day
|
cause of death
Time Frame: 1 day
|
cause of death
|
1 day
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: Pierre Fesler, PUPH, UH Montpellier
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- RECHMPL21_0188
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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