- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03293966
A Coordination Card of Care Relative to the Medicinal Treatments Got Out of it From Hospitalization
Therapeutic CARE of the Bronchial Cancer Not in Small Cell: Security of the Dispensation of Medicine by the Implementation of a Card of Coordination of Care Relative to the Medicinal Treatments Got Out of it From Hospitalization
The continuity of the medicinal care between the city and the hospital stays a major organizational stake and of safety of patients' therapeutic care.This takeover is more complex when it concerns pathology needed lots of hospitalization and included the intervention of multiple healthcare practionners. This is clearly the case of cancer coverage.
The optimization of the therapeutic suppor in town is based on pharmaceutical advice strengthening but also on the pharmaceutical analysis to check the entire treatments' prescription and eventual medicinal interactions which ensue from it.That's why it's important to have a medicinal conciliation that takes into account all the medecine taken or have to be taken by the patient.
A specific support was developped by nurses , doctors and pharmacist ; it's a care coordination card that can be put easely in a pocket by the patient.
The aim of the study is that this card can be also used as a communication tools by sharing the prescription done at the release of hospital by using an IT link (flea datamatrix) for the patients Via the use of an IT link (flea datamatrix) for the patients whose pathology is complex in term of extra hospital coverage.
Study Overview
Status
Conditions
Detailed Description
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Ile-de-France
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Paris, Ile-de-France, France, 75014
- Groupe Hospitalier Paris Saint Joseph
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
All patients admitted to thoracic pneumology and oncology treated with anticancer drugs will receive a medication conciliation.
Patients integrating the study will be patients who have benefited from the entire process of medication conciliation (entry and exit) and returning home.
The included patients must have attended the same pharmacy for at least 3 months (according to the patient declaration).
Description
Inclusion Criteria:
- all patient admitted in onco-thoracic service
- Handled by an anticancer agent
- Having frequented the same city pharmacy for at least 3 months
Exclusion Criteria:
- hospitalization above 21 days
- refusing participation
- palliative care
- misunderstanding of french language
- frequenting several pharmacy
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
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Composite criteria including all the dysfunctions noticed at the release of the hospital prescription intended to be dispensed in town.
Time Frame: 7days+/- 2 days
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7days+/- 2 days
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- PRIMACIE
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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