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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03393299
Other study ID # RC-P0059
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 16, 2018
Est. completion date October 30, 2018

Study information

Verified date August 2020
Source Lille Catholic University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Assess the impact of the systematic use of STOPP/START tool during medication conciliation on the evolution of hospitalised elderly people's quality of life at 2 months.


Recruitment information / eligibility

Status Completed
Enrollment 65
Est. completion date October 30, 2018
Est. primary completion date July 17, 2018
Accepts healthy volunteers No
Gender All
Age group 75 Years and older
Eligibility Inclusion Criteria:

- Patient with more than 75 years old

- Hospitalized in geriatrics short-stay

- Patient with a written informed consent

- Patient with a social security scheme

Exclusion Criteria:

- Severe dementia

- Not able to respond to SF-12

- Disease at final stage

- Patient under legal protection (maintenance of justice, tutelage, legal guardianship)

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
STOPP/START criteria
software which helps to do the drug reconciliation

Locations

Country Name City State
France Hôpital La Porte Verte Versailles

Sponsors (1)

Lead Sponsor Collaborator
Lille Catholic University

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary SF-12 Quality of life scale The evolution of the hospitalised elderly people's quality of life at 2 months will be measured by the SF-12 scale. at inclusion and at 2 months
Secondary Number of falls The number of falls during the two months following the inclusion will be collected for each patient. at 2 months
Secondary Proportion of patients rehospitalized The proportion of patients that have been rehospitalized (unscheduled hospitalization) during the two months following inclusion will be measured. at 2 months
Secondary Mortality The mortality during the two months following inclusion will be measured. at 2 months
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