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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03636711
Other study ID # 2018-24
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date September 2018
Est. completion date January 2022

Study information

Verified date August 2018
Source Assistance Publique Hopitaux De Marseille
Contact PHILIPPE PAROLA, MD
Phone +33 491387235
Email Philippe.PAROLA@ap-hm.fr
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Consensual antibiotic protocols have been developed and validated locally by infectious disease specialists, internists and emergency physicians, in order to encourage their compliance. A preliminary study was conducted from June 2015 to February 2016, including 622 patients admitted to the emergency department for infectious syndrome such as /

- Pneumoniae

- Urinary tract infection

- Cellulitis

- Meningitis

- Malaria

- Febrile neutropenia

- Febrile acute diarrhea

- Fever back to the tropics

- Angina

- sexually transmitted infection This prospective study will observe and analyze the adherence of prescribers to these protocols. With description of patients who benefited or not the antibiotic protocol, according to a syndromic approach and analysis of the causes of non-adherence to the protocols. In order to limit the length of stay and reduce the cost of hospitalization..


Description:

Consensual antibiotic protocols have been developed and validated locally by infectious disease specialists, internists and emergency physicians, in order to encourage their compliance. A preliminary study was conducted from June 2015 (setting up protocols) to February 2016, including 622 patients admitted to the emergency department for infectious syndrome such as /

- Pneumoniae

- Urinary tract infection

- Cellulitis

- Meningitis

- Malaria

- Febrile neutropenia

- Febrile acute diarrhea

- Fever back to the tropics

- Angina

- sexually transmitted infection This prospective study will observe and analyze the adherence of prescribers to these protocols. With description of patients who benefited or not the antibiotic protocol, according to a syndromic approach and analysis of the causes of non-adherence to the protocols. In order to limit the length of stay and reduce the cost of hospitalization..


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 2000
Est. completion date January 2022
Est. primary completion date July 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patient admitted to emergency for infectious syndrome

- Patient > 18 years old.

- Patient who accept to have his medical records reviewed for research.

Exclusion Criteria:

- Patient < 18 years old.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
antibiotic protocol, according to a syndromic approach
Description of patients who benefited or not the antibiotic protocol, according to a syndromic approach and analysis of the causes of non-adherence to the protocols

Locations

Country Name City State
France Assistance Publique Des Hopitaux de Marseille Marseille Paca

Sponsors (1)

Lead Sponsor Collaborator
Assistance Publique Hopitaux De Marseille

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary List of Antibiotic treatment Description of the prescribed antibiotic treatment depending of infectious syndrome: name, duration for each treatment during hospitalization
Data will be collected in the medical files:
date of introduction of antibiotic treatment
withdrawal dates
stop dates
antibiotic classes
up to 12 weeks
Primary Adverse events Description of the cause of non adherence to antibiotic treatment initiates at hospital admission of antibiotherapy:
Data will be collected in the medical files of patients:
events leading to withdrawal or stop treatment (insufficiency renal, allergic reaction ... etc) date of events aggravation or recovery
up to 12 weeks
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