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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02852733
Other study ID # 35RC12_8988
Secondary ID
Status Completed
Phase N/A
First received July 25, 2016
Last updated August 1, 2016
Start date June 2014
Est. completion date June 2015

Study information

Verified date July 2016
Source Rennes University Hospital
Contact n/a
Is FDA regulated No
Health authority France: Commission nationale de l'informatique et des libertés (CNIL)France : Comité consultatif sur le traitement de l'information en matière de recherche (CCTIRS)
Study type Observational

Clinical Trial Summary

The purposes of this study are :

- To know and to understand frequency and variability (quantitative and qualitative) of end-of-life emergencies in nursing homes.

- To know and to understand practices applied in these situations depending on the institution and the different reasons of hospital use.

- To know and to understand the practical and organizational elements, in nursing homes, that can determine a (re) hospitalization or an end-of-life


Recruitment information / eligibility

Status Completed
Enrollment 602
Est. completion date June 2015
Est. primary completion date February 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- dead residents during the quarter preceding the date of the Survey Or

- Residents in end-of-life situation the day of the survey, as determined by the physician coordinator of nursing homes (we will use the definition of "terminal condition" contained in the guide of the CNSA (coding PATHOS - April 2011)).

Exclusion Criteria:

- patients opposing the study,

- patients aged below 18 year old

Study Design

Observational Model: Cohort


Related Conditions & MeSH terms


Intervention

Other:
end-of-life emergencies' management


Locations

Country Name City State
France CHU de RENNES Rennes

Sponsors (1)

Lead Sponsor Collaborator
Rennes University Hospital

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary number of end-of-life emergencies' episodes through study completion, an average of 1 year No