- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving 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.
Studieoversikt
Status
Forhold
Detaljert beskrivelse
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.
Studietype
Registrering (Faktiske)
Kontakter og plasseringer
Studiesteder
-
-
-
Paris, Frankrike
- Lariboisière Hospital
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Prøvetakingsmetode
Studiepopulasjon
Beskrivelse
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
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Observasjonsmodeller: Kohort
- Tidsperspektiver: Potensielle
Kohorter og intervensjoner
Gruppe / Kohort |
|---|
|
Patients aged 80 years and older
Patients aged 80 years and older and hospitalized in a cardiology department
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Percentage of patients for which national guidelines were followed
Tidsramme: 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
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Percentage of patients aged 80 and older hospitalized in the university and non university
Tidsramme: 1 day
|
Better understand the demographics of cardiology services in France (Demography)
|
1 day
|
Samarbeidspartnere og etterforskere
Sponsor
Publikasjoner og nyttige lenker
Studierekorddatoer
Studer hoveddatoer
Studiestart (Faktiske)
Primær fullføring (Faktiske)
Studiet fullført (Faktiske)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Anslag)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- 09472
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Studerer et amerikansk FDA-regulert enhetsprodukt
produkt produsert i og eksportert fra USA
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .