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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02011009
Other study ID # 13-PP-02
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 2013
Est. completion date January 2016

Study information

Verified date December 2013
Source Centre Hospitalier Universitaire de Nice
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Bacterial resistance to antibiotics is a major public health problem. The epidemiology of enteric bacteria including E. coli is changing rapidly with the global spread of a resistance mechanism type beta-lactamase extended spectrum (ESBL), responsible for resistance to almost all penicillins and cephalosporins. The resistance is up to 75% for Quinolones, 67% for Cotrimoxazole and 30-50% for Aminoglycosides.

The main phenomena causing this problem are:

- The selection pressure by antibiotics, in their use in humans or animals

- The hand transmission via the digestive reservoir (faeces)

- Easy spread of resistance mechanism in Enterobacteriaceae due to transferable genetic support (plasmid)

In this context, we decided to implement a cross-border study to improve and accelerate the management, diagnosis and treatment of patients with ESBL in close collaboration between medical and paramedical staff in hospitals, laboratories and private medical offices.

The objective of this study is to standardize diagnostic and therapeutic measures allowing a better and rapid treatment of patients and thus prevent the appearence of ESBL bacteria in the PACA region and Liguria by providing a tool : The "Kit ESBL".

The " ESBL ToolKIT" (also translated into Italian) includes:

- Information on epidemiological data

- A checklist edited for extra-hospital use (private practitioners, health care units other than hospitals)

- A checklist edited for hospital use

- A leaflet BMR for the patient explaining the problematic as well as hygiene measures

- Therapeutical protocols for hospital use and extra hospital use

- An sample letter for the attending physician

The objective of this prospective multicenter cohort study is to evaluate the use of this kit, and to measure its impact on:

- The prescription of appropriate antibiotics

- The measures taken to prevent man to man transmission

- The quality of information provided to the patient

In this context we are also performing a multicentre prospective interventional cohort of HIV+ patients searching for possible sexual transmission factors in ESBL (extended-spectrum ß-lacatamase-producing bacteria) carriers.

We will also try to determine if other sexually transmitted infections associated (syphilis, gonorrhea and chlamydia) are contributing factors to ESBL carriage.

So far there is no data documented on ESBL-carriage in a population of HIV-positive patients.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date January 2016
Est. primary completion date November 2015
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Age > 18

- HIV+ patient of the hospital's outpatient clinic

- Signature of informed consent

- Affiliation of the Social Security system

Exclusion criteria

- Vulnerable Persons: minor patient, wardship (tutelage), no liberty to act and speak

- Pregnancy and lactation: a urine pregnancy test will be performed for women of childbearing age. Results will be reported by the physician selected by the patient

Study Design


Related Conditions & MeSH terms


Intervention

Other:
HIV seropositive patients
During a routine visit, a self-administered anal swab will be proposed as well as an anonymous questionnaire about sexual practices. In addition to usual outpatient treatment an examination and an evaluation of a possible sexually transmitted infection (STI) will be realized. Some questions about risk factors traditionally associated with carriage of resistant bacteria will also be investigated with the aid of the questionnaire such as: use of antibiotics during the year, travel in areas at risk.

Locations

Country Name City State
France MONDAIN Nice Alpes-Maritimes

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire de Nice

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary enterobacteria ESBLs measure the carriage of antibiotic-resistant bacteria in HIV seropositive patients looking for potential factors associated with sexual transmission. baseline
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