- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05045235
Optimization of Drug Prescriptions in the Care Pathway for the Elderly, With the Final Objective of Reducing the Iatrogenic Risk (IATROPREV)
February 7, 2023 updated by: Centre Hospitalier Universitaire, Amiens
Optimization of Drug Prescriptions in the Care Pathway for the Elderly, With the Final Objective of Reducing the Iatrogenic Risk.
The IATROPREV project is an organizational innovation experimentation project, carried out in Hauts-de-France by the University hospitals of Amiens and Lille, the ARS and the URPS Doctors and Pharmacists of Hauts-de-France and following to the social security financing law of 2018, allowing experimentation with new organizations in the health sector, according to article 51.
The objectives of this course are to improve the relevance of prescription in elderly people with multiple drugs as well as, the coordination of care between the city and the hospital through the sharing of information and the establishment of multi-professional consultations between the various care actors.
Study Overview
Status
Recruiting
Conditions
Study Type
Observational
Enrollment (Anticipated)
1500
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: Frédéric BLOCH, MD
- Phone Number: 03 22 45 57 20
- Email: bloch.frederic@chu-amiens.fr
Study Locations
-
-
-
Amiens, France, 80054
- Recruiting
- Amiens University Hospital
-
Contact:
- Frédéric BLOCH, MD
- Phone Number: 03 22 45 57 20
- Email: bloch.frederic@chu-amiens.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
- ADULT
- OLDER_ADULT
- CHILD
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
patient hospitalized in the geriatric medicine department with olymedicated drugs
Description
Inclusion Criteria:
- patient hospitalized in the geriatric medicine department
- Potential involvement of a drug in hospitalization or potential or proven iatrogenic event during hospitalization;
- Numerous therapeutic modifications (3 or more);
- Drug interaction or introction of a new drug with one or more drug interactions;
- Medicinal product with a narrow therapeutic marge drug requiring close monitoring.
Exclusion Criteria:
- patient non hospitalized in the geriatric medicine department
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 |
Measure Description |
Time Frame |
---|---|---|
Change of side effect number in ederly with polymedicated drugs
Time Frame: up to 4 years
|
Change of side effect number in ederly with polymedicated drugs
|
up to 4 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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)
September 1, 2021
Primary Completion (ANTICIPATED)
September 1, 2025
Study Completion (ANTICIPATED)
September 1, 2025
Study Registration Dates
First Submitted
September 7, 2021
First Submitted That Met QC Criteria
September 7, 2021
First Posted (ACTUAL)
September 16, 2021
Study Record Updates
Last Update Posted (ACTUAL)
February 8, 2023
Last Update Submitted That Met QC Criteria
February 7, 2023
Last Verified
February 1, 2023
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- PI2021_843_0158
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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