Effect of the Use of a Therapeutic Conciliation Document at the Outlet of Hospital, on the Emergency Use of Hospital Care in Patient Aged Over 75 Years Old.
NCT ID: NCT02916836
Last Updated: 2018-02-19
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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WITHDRAWN
OBSERVATIONAL
2017-01-31
2020-01-31
Brief Summary
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Detailed Description
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To do this, we are proposing a multicenter observational study. Randomization would be across the centres. The study would focus on 750 patients more of 75 with polymedication. The follow-up will last 6 months.
The main objective will be to determine if the use of the TDC, at the discharge of hospital, allows to reduce the number of use in emergency care within the two month after their hospital discharge. The first secondary objective will be identical to the main objective but rated at 6 months and the second secondary objective will be to assess the impact of the use of the TDC on overall mortality at 6 months.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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With TDC sheet
Use of therapeutic drug conciliation sheet (TDC) by the hospital and transmitted to the family practitioner with other usual documentation
therapeutic drug conciliation sheet (TDC)
Use of therapeutic drug conciliation sheet (TDC)
Without TDC Sheet
transmission of usual documentation only to the family practitioner
No Use of therapeutic drug conciliation sheet (TDC)
Interventions
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therapeutic drug conciliation sheet (TDC)
Use of therapeutic drug conciliation sheet (TDC)
No Use of therapeutic drug conciliation sheet (TDC)
Eligibility Criteria
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Inclusion Criteria
* patients with a medical prescription, including at least three different allopathic molecules including at least a treatment in one of the following therapeutic classes:
* cardiovascular treatment: antiarrhythmics, antihypertensive drugs, anticoagulants and antiplatelet all classes
* treatment of the central nervous system: analgesics, benzodiazepines, antidepressants, hypnotic, antipsychotic drugs of all classes.
* family practitioner identified
* trusted personne identified
* Hospital output project establishes
Exclusion Criteria
* short survival time
75 Years
ALL
No
Sponsors
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Centre Hospitalier Universitaire de Nice
OTHER
Responsible Party
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Principal Investigators
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Olivier GUERIN
Role: PRINCIPAL_INVESTIGATOR
Centre Hospitalier Universitaire de Nice
Other Identifiers
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14-PREPS-01
Identifier Type: -
Identifier Source: org_study_id
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