Elderly Clinical Trial - Iatrogenic Drug Risk in People NCT03686943

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number	NCT03686943
Other study ID #	RIPH3-RNI18 / RIMPAP
Secondary ID	2018-A02122-53
Status	Withdrawn
Phase
First received
Last updated
Start date	June 28, 2019
Est. completion date	June 28, 2019

Study information
Verified date	September 2019
Source	University Hospital, Tours
Contact	n/a
Is FDA regulated	No
Health authority
Study type	Observational

Clinical Trial Summary

Many hospitalizations or emergency room visits are due to problems of iatrogenic medication, especially in elderly patients who are very often polymedicated. Moreover, they are more at risk because of fragility. This has an important socio-economic impact. It therefore seems important to act upstream of these adverse events and a review of the drugs available in the homes of elderly patients seems a good starting point.

Recruitment information / eligibility
Status	Withdrawn
Enrollment	0
Est. completion date	June 28, 2019
Est. primary completion date	June 28, 2019
Accepts healthy volunteers	Accepts Healthy Volunteers
Gender	All
Age group	75 Years and older
Eligibility	Inclusion Criteria: - Patient over 75 years with or without cognitive disorders Exclusion Criteria: - Refusal to participate

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Family pharmacy
Observation of the family pharmacy in elderly group

Locations
Country	Name	City	State
n/a

Sponsors *(1)*
Lead Sponsor	Collaborator
University Hospital, Tours

Outcome
Type	Measure	Description	Time frame	Safety issue
Primary	Iatrogenic drug risk in patients' homes	Description of potential drug contraindications and potential unadvisable drug interactions highlighted from the analysis of the family pharmacy by Theriaque databased	At the inclusion (baseline)

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Iatrogenic Drug Risk in People Over 75, With or Without Cognitive Disorders, From an Inventory of Their Family Pharmacy

Clinical Trial Details — Status: Withdrawn

Administrative data

Study information

Clinical Trial Summary

Recruitment information / eligibility

Study Design

Related Conditions & MeSH terms

Intervention

Locations

Sponsors (1)

Outcome