- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03985332
Evolution of the Rate and Causes of Death in Geriatric SSR
September 30, 2019 updated by: University Hospital, Strasbourg, France
Epidemiological Study on the Evolution of the Rate and Causes of Mortality in Geriatric SRH in the HUS
In view of the ageing population and the increasing fragility of geriatric patients, it seems interesting to carry out a retrospective epidemiological observational study, on the evolution of the mortality rate and the causes of death in services of suite care and geriatric rehabilitation, in order to apprehend at best the supports, in particular palliative
Study Overview
Status
Unknown
Conditions
Study Type
Observational
Enrollment (Anticipated)
100
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Thomas VOGEL, MD, PhD
- Phone Number: 33 3 88 11 54 74
- Email: thomas.vogel@chru-strasbourg.fr
Study Contact Backup
- Name: Candice MULLER, MD
- Phone Number: 33 3 88 11 54 74
- Email: candice.muller@chru-strasbourg.fr
Study Locations
-
-
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Strasbourg, France, 67091
- Recruiting
- Service Gériatrie
-
Sub-Investigator:
- Candice MULLER, MD
-
Contact:
- Thomas VOGEL, MD, PhD
- Phone Number: 33 3 88 11 54 74
- Email: thomas.vogel@chru-strasbourg.fr
-
Principal Investigator:
- Thomas VOGEL, MD, PhD
-
Contact:
- Candice MULLER, MD
- Phone Number: 33 3 88 11 54 74
- Email: candice.muller@chru-strasbourg.fr
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
All patients who died during their stay in geriatric SSR between 01/01/2013 and 31/12/2017
Description
Inclusion Criteria:
- Major patients (≥ 18 years)
- All patients who died during their stay in geriatric SSR between 01/01/2013 and 31/12/2017
- Patients who have not expressed their living refusal to reuse their medical data for research purposes
Exclusion Criteria:
- Refusal on the part of patients of their living to reuse their medical data for research purposes
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Study of the different causes of death in geriatric SSR unit
Time Frame: The period from January 1st, 2013 to December 31st, 2017 will be examined
|
The period from January 1st, 2013 to December 31st, 2017 will be examined
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Director: Thomas VOGEL, MD, PhD, University Hospital, Strasbourg, France
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
June 15, 2019
Primary Completion (Anticipated)
May 1, 2020
Study Completion (Anticipated)
May 1, 2020
Study Registration Dates
First Submitted
April 29, 2019
First Submitted That Met QC Criteria
June 11, 2019
First Posted (Actual)
June 13, 2019
Study Record Updates
Last Update Posted (Actual)
October 3, 2019
Last Update Submitted That Met QC Criteria
September 30, 2019
Last Verified
April 1, 2019
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 7375
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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