Efficacy and Cost-effectiveness of Hospital Antimicrobial Stewardship Programs (CEFECA)
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|ClinicalTrials.gov Identifier: NCT02814877|
Recruitment Status : Unknown
Verified July 2017 by Assistance Publique - Hôpitaux de Paris.
Recruitment status was: Recruiting
First Posted : June 28, 2016
Last Update Posted : July 5, 2017
|Condition or disease||Intervention/treatment|
|Antimicrobial Resistance||Other: promotion of appropriate use of antibiotics in hospital|
Show Detailed Description
|Study Type :||Observational|
|Estimated Enrollment :||30 participants|
|Observational Model:||Ecologic or Community|
|Official Title:||Efficacy and Cost-effectiveness of Hospital Antimicrobial Stewardship Programs|
|Actual Study Start Date :||September 2016|
|Estimated Primary Completion Date :||September 2017|
|Estimated Study Completion Date :||December 2017|
- Other: promotion of appropriate use of antibiotics in hospital
promotion of appropriate use of antibiotics in hospital by visiting physicians
- Evaluate the efficacy and the cost-effectiveness of strategies to promote appropriate use of antibiotics in hospitals and identify the most efficient ones, on a short-term but also long-term scale. [ Time Frame: 12 months ]A comparison of the different strategies based on the incremental cost-effectiveness ratio (ICER), which is defined by the difference in costs between interventions, divided by the difference in their measured impact
- to map the different antimicrobial stewardship setups in french hospital [ Time Frame: 12 months ]accrue high-value information in the field of antibiotic stewardship,
- to measure prescribers' adherence to the different strategies used to control antibiotic description [ Time Frame: 12 months ]namely physicians' adherence to antibiotic counselling and interventions to control its use for the effective implementation of such programs.
- to identify potential barriers and facilitators to the implementation of effective stewardship programs [ Time Frame: 12 months ]namely physicians' adherence to antibiotic counselling and potential barriers and facilitators for the effective implementation of such programs.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02814877
|Contact: Jean Christophe LUCET, PHD||1 40 25 61 94 ext firstname.lastname@example.org|
|Contact: Anne Perozziello||1 40 25 61 94 ext email@example.com|
|Contact: anne perozziello firstname.lastname@example.org|
|Principal Investigator:||Jean Christophe LUCET||APHP|