Actively Recruiting

Phase Not Applicable
Age: 65Years +
All Genders
NCT05475574

Impact of Discontinuing Contact Precautions for Extended-spectrum β-lactamase Enterobacteriaceae in a Geriatric Unit

Led by Centre Hospitalier Régional Metz-Thionville · Updated on 2025-04-27

954

Participants Needed

1

Research Sites

341 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This is an interventional multicenter prospective noninferiority non-randomized double-blind controlled before and after study. The aim of this study is to demonstrate that standard precautions alone are not inferior to contact precautions by comparing the incidence density of extended-spectrum β-lactamase (ESBL)-producing Enterobacteriaceae acquired in geriatric units before and after discontinuing contact precautions.

CONDITIONS

Official Title

Impact of Discontinuing Contact Precautions for Extended-spectrum β-lactamase Enterobacteriaceae in a Geriatric Unit

Who Can Participate

Age: 65Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patient (> 65 years old)
  • Patient hospitalized in geriatrics during the study period
  • Free and informed consent obtained from the patient (or his trusted person or legal representative) within 48 hours of admission at the geriatric unit
  • Patient affiliated to a social security scheme
Not Eligible

You will not qualify if you...

  • Patient requiring contact precaution for an indication other than ESBL during the stay (COVID-19, classical PCC excluding ESBL, Clostridium difficile PCC, scabies PCC, BHRe PCC)
  • Patient's stay period less than 4 days
  • Patient under legal protection
  • Person deprived of liberty

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

CHR Metz-Thionville/Hôpital Bel Air

Metz, France, 57085

Actively Recruiting

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Research Team

L

Laurie RENAUDIN, MD

CONTACT

M

Mathieu LLORENS, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

PREVENTION

Number of Arms

2

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