Depression in Old Age Clinical Trial
— BZDOfficial title:
Study of the Reduction of the Prescriptions of Benzodiazepines and Related After the Discharge of a Service of Follow-up Care and Geriatric Rehabilitation
NCT number | NCT06107283 |
Other study ID # | 8787 |
Secondary ID | |
Status | Recruiting |
Phase | |
First received | |
Last updated | |
Start date | March 1, 2023 |
Est. completion date | August 17, 2024 |
Verified date | October 2023 |
Source | University Hospital, Strasbourg, France |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The significant consumption of Benzodiazepines and related drugs in the elderly outside of good practice recommendations is a major issue in the care of the elderly. Adverse effects have been the subject of numerous studies, leading to falls, addictions and even deaths. The general practitioner is often faced with long-term medication intake which is not consistent with a good benefit/risk balance, but stopping or reducing the dosage remains a problem in current practice. The Aftercare and Geriatric Rehabilitation services due to their operation (several weeks of hospitalization) seek to adapt the patient's therapies in order to obtain the most convincing benefit/risk balance possible. A reduction or withdrawal of treatments with Benzodiazepines or related drugs are therefore frequently initiated.
Status | Recruiting |
Enrollment | 150 |
Est. completion date | August 17, 2024 |
Est. primary completion date | August 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 75 Years and older |
Eligibility | Inclusion Criteria: - Major subject (= 75 years old) - Subject discharged from a geriatric Follow-up Care and Rehabilitation service for whom a reduction in the dosage of Benzodiazepines and related drugs was carried out during hospitalization and who returned home (individual or EHPAD) after hospitalization. - Subject not opposing, after information, the reuse of their data for the purposes of this research. Exclusion Criteria: - Subject having expressed opposition to participating in the study. - Subject having treatment with Benzodiazepine to prevent recurrence of epileptic seizures. |
Country | Name | City | State |
---|---|---|---|
France | Gériatrie - Service de Soins de Soins Médicaux et de Réadaptation - CHU de Strasbourg - France | Strasbourg |
Lead Sponsor | Collaborator |
---|---|
University Hospital, Strasbourg, France |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The number of patients who had an increase in Benzodiazepines in the 12 weeks following discharge from hospitalization. | 12 weeks following discharge from hospitalization. |
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