Clinical Trials Logo

Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03226314
Other study ID # 2015/CHU/14
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date November 21, 2017
Est. completion date June 30, 2019

Study information

Verified date March 2019
Source Centre Hospitalier Universitaire de la Réunion
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

In its report dated april 2014, World Health Organization confirms antibiotic resistance dissemination in all parts of the world, in hospitals and in community and worries about a possible comeback to a pre-antibiotic era during the 21st century. For the last 15 years, third-generation cephalosporins resistant enterobacteriaceae (3GCREB) prevalence is continuously increasing. Community 3GCREB prevalence has not been studied whereas several observations made in Reunion Island hospital suggest a diffusion in community. In this situation of world-wide and regional extension of bacterial resistance, the investigator offers to study bacterial resistance to antibiotic in Reunion Island community.


Description:

The investigator is focused on E. coli species exhibiting BLSE or metallo-betalactamases production that could be encountered du to the increasing level of migratory flow in Reunion Island.

Fecal sample collection will be used for further investigations on bacterial typology.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 500
Est. completion date June 30, 2019
Est. primary completion date December 1, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

Patients:

- aged over 18 years old

- admitted in emergency ward or intensive care of the university hospital of Reunion Island

- who received the patient information notice and who gave their consent

- who have a stool sample performed in the 48 hours following admission

- who understand and can read French

Exclusion Criteria:

Patients:

- transferred from a short-term, middle-term or long-term stay health facility

- who have a stool sample performed more than 48 hours following admission.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
stool sample
study will be proposed to all patients entering emergency ward or intensive care unit in Reunion Island university hospital. Upon consent, a stool sample will be taken (either directly on emitted stools or by rectal sampling) and analysed for enterobacteriaceae.

Locations

Country Name City State
Réunion Chu Reunion Island Saint-Pierre Reunion Island

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire de la Réunion

Country where clinical trial is conducted

Réunion, 

Outcome

Type Measure Description Time frame Safety issue
Primary Digestive prevalence rate of 3GCREB estimate of digestive prevalence rate of 3GCREB in participating patients and extrapolation to Reunion Island community population. through study completion, an average of 1 day
See also
  Status Clinical Trial Phase
Completed NCT02223338 - Bacterial Resistance in Patients Receiving Post-Intravitreal Injection Antibiotics N/A
Active, not recruiting NCT01208519 - SATURN 04 Nosocomial Acquisition Study N/A
Completed NCT03998865 - Bacterial Microbiota Characterization on Implant-supported PEEK and Titanium Provisional Abutments N/A
Not yet recruiting NCT03752476 - Impact of Number of Rank of B-lactam Antibiotics on Emergence on Multidrug Resistant Bacteria
Completed NCT05939479 - Antistaphylococcal Betalactam and Emergence of Resistance
Completed NCT02641015 - Study to Assess Management and Outcomes of Hospitalised Patients With Complicated UTI (RESCUING) N/A
Completed NCT01878643 - Reduction of Bacterial Resistance With Inhaled Antibiotics in the Intensive Care Unit Phase 0