- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06026241
Practice Analysis of Care, Paraclinical Exams and Treatments Received by Geriatric Patients Both During the Last Week and the Last 24 Hours of Their Lives.
March 7, 2024 updated by: Centre Hospitalier Universitaire de Saint Etienne
End-of-life care is a core topic for geriatricians.
One of the key aspects of end-of-life management is deciding when to discontinue active care measures (for example blood pressure monitoring, blood tests and X-rays) in favor of exclusive comfort care.
In this retrospective observational study, the investigators looked at the care measures, treatments and paraclinical exams received by geriatric patients both one week and 24 hours before their death.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
This analysis provides information on the differences in geriatric physicians' practices regarding the anticipation of the end of life, by showing on average when active care measures were stopped before death.
Secondly, the investigators looked at patient criteria that could explain a prolongation of active care and a delay in the implementation of exclusive comfort care.
Study Type
Observational
Enrollment (Estimated)
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: Ludovic LAFAIE, MD
- Phone Number: +33 (0)477127397
- Email: ludovic.lafaie@chu-st-etienne.fr
Study Contact Backup
- Name: Solène VALETTE, resident
- Phone Number: +33 (0)670511373
- Email: solene.valette@hotmail.fr
Study Locations
-
-
-
Saint-Étienne, France
- Recruiting
- CHU Saint-Etienne
-
Sub-Investigator:
- Ludovic LAFAIE, MD
-
Contact:
- Ludovic LAFAIE, MD
- Phone Number: +33 (0)477127397
- Email: ludovic.lafaie@chu-st-etienne.fr
-
Contact:
- Solène VALETTE, resident
- Phone Number: +33 (0)670511373
- Email: solene.valette@hotmail.fr
-
Principal Investigator:
- Solène VALETTE, resident
-
-
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
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
All patients over 75 years old who died in the geriatric short-stay departments of Saint-Etienne University Hospital
Description
Inclusion Criteria:
- All patients over 75 years old who died in a geriatric short-stay department at Saint-Etienne University Hospital.
Exclusion Criteria:
- Patients under 75 years old
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Patients over 75 who died in geriatrics
Patients over 75 years old who died in the geriatric short-stay departments of Saint-Etienne University Hospital
|
Patient's socio-demographic data (age, gender, residence), comorbidities, cause of death, date and frequency of care measures/treatments/paraclinical exams received before their death.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Prevalence of care and treatments received during the last week of life, and during the last 24 hours of life
Time Frame: In the last week of life and 24 hours before death
|
To measure the prevalence of care (hemodynamic, biological and radiological monitoring), and to evaluate the treatments received during the last week of life, and during the last 24 hours of life of patients hospitalized and who died in a geriatric short-stay ward.
|
In the last week of life and 24 hours before death
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Patient criteria that may have explained the pursuit of care
Time Frame: In the last week of life and 24 hours before death
|
Analysis of patient criteria (age, comorbidities, etc.) that may have explained the continuation of care, treatments and paraclinical exams up to the last 24 hours before death.
|
In the last week of life and 24 hours before death
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Ludovic LAFAIE, MD, CHU Saint-Etienne
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)
March 1, 2024
Primary Completion (Estimated)
December 31, 2025
Study Completion (Estimated)
December 31, 2025
Study Registration Dates
First Submitted
August 30, 2023
First Submitted That Met QC Criteria
August 30, 2023
First Posted (Actual)
September 7, 2023
Study Record Updates
Last Update Posted (Actual)
March 8, 2024
Last Update Submitted That Met QC Criteria
March 7, 2024
Last Verified
March 1, 2024
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- IRBN1162023/CHUSTE
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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