- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01121679
French Observatory on Hospitalizations in Cardiology of Patients of 80 Years and Over (OCTOCARDIO)
Because of increased life expectancy and improved therapeutic methods in cardiology, the proportion of very old patients with cardiovascular disease increases. However, clinical practice "in real life" are still insufficiently known in this population. The recommendations still lack of studies specifically devoted to elderly or very elderly, an extrapolation of data based on evidence obtained in younger populations.
This is a multicenter observational study during a day. On this day, all participating centers fill a questionnaire for each patient 80 years or older hospitalized in their service.
Study Overview
Status
Conditions
Detailed Description
Information about the center will be collected: non-university or university center, presence of coronary angiography room, number of beds, number of patients 80 years or older hospitalized in the day of the investigation.
The questionnaire is designed to:
- Know the history of cardiovascular and noncardiovascular patient and degree of dependence
- Know the reason for hospitalization
- Evaluate the diagnostic and therapeutic already implemented or planned for this patient
The day of the survey, information on each patient 80 years or older hospitalized in the service will be collected:
- Patient Data: date of birth, sex, status. The patient identification data (name, surname, address) will not be collected.
- Patient History: date of last hospitalization, life, cardiovascular risk factors, cardiovascular and non cardiovascular history, date of last hospitalization, life
- Circumstances of admission: course of care before admission, admission to intensive care unit or hospital unit classical primary diagnosis and diagnosis (s) partner (s)
- Initial assessment: treatment admission, major hemodynamic, electrocardiographic and biological
- Regarding the current hospitalization: diagnosis already implemented or planned (echocardiography, angiography, electrophysiological study, etc ...), therapeutic methods already implemented or planned angioplasty, percutaneous valve intervention, conventional or biventricular stimulation, cardiac surgery, medication
- Become of the patient after hospitalization
- The clinician's subjective impressions about the condition of the patient and monitoring recommendations
- Assessment of addiction: ADL Scale
No monitoring of patients is contemplated.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
Paris, France
- Lariboisiere Hospital
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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:
- Patient aged 80 years or more
- Patient present in a cardiology service in the morning (8:00 to 12:00) the day of the survey
- Admission to the service took place on the survey day or in the 15 days preceding the survey.
Exclusion Criteria:
- Patient with age <80 years.
- Patient who have expressed a refusal to participate in the study
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
|---|
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Patients aged 80 years and older
Patients aged 80 years and older and hospitalized in a cardiology department
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Percentage of patients for which national guidelines were followed
Time Frame: 1 day
|
Evaluate clinical practice and particularly the monitoring of recommendations of international scientific societies in the population of very elderly (≥ 80 years)
|
1 day
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Percentage of patients aged 80 and older hospitalized in the university and non university
Time Frame: 1 day
|
Better understand the demographics of cardiology services in France (Demography)
|
1 day
|
Collaborators and Investigators
Sponsor
Publications and helpful links
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 (Estimate)
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
- 09472
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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