Actively Recruiting

Phase Not Applicable
Age: 65Years +
All Genders
ID05475574

Impact of Discontinuing Contact Precautions for Extended-spectrum Beta-lactamase Enterobacteriaceae in a Geriatric Unit: An Interventional Prospective Noninferiority Double-blind Controlled Before and After Study

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

954

Participants Needed

1

Research Sites

2 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating whether stopping contact precautions is as safe as continuing them in preventing infections caused by extended-spectrum beta-lactamase (ESBL)-producing Enterobacteriaceae in older adults hospitalized in geriatric units. This study is designed as a prospective, non-randomized, double-blind controlled before and after study to compare infection rates before and after discontinuing contact precautions. The study addresses a significant concern as these infections are common in healthcare settings and limit treatment options. Participants will be observed during two study phases: one with the use of contact precautions alongside standard precautions for patients carrying ESBL-producing bacteria, and another phase after stopping contact precautions where only standard precautions are used. The study involves comparing the incidence density of acquired ESBL infections over a six-month period in a geriatric hospital setting. Throughout the study, participants' infection status will be monitored and healthcare workers' compliance with hand hygiene and protective equipment use will be assessed. Patient satisfaction related to care will also be evaluated using questionnaires at discharge. This monitoring includes safety evaluations and adherence tracking, with follow-up assessments conducted during and after the six-month observation periods.

CONDITIONS

Brief 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 older than 65 years
  • Patient hospitalized in geriatrics during the study period
  • Free and informed consent obtained from the patient or their trusted person or legal representative within 48 hours of admission
  • Patient affiliated with a social security scheme
Not Eligible

You will not qualify if you...

  • Patient requiring contact precautions for infections other than ESBL (such as COVID-19, Clostridium difficile, scabies, or other listed infections) on admission or during the stay
  • Patient under legal protection
  • Person deprived of liberty
  • Patient with a hospital stay shorter than 4 days

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Observation with Contact Precautions

Duration - 6 months

Participants are observed during a period when contact precautions are applied in addition to standard precautions for any patient carrying ESBL-producing Enterobacteriaceae.

Regular assessments during hospital stay up to 6 months

Observation without Contact Precautions

Duration - 6 months

Participants are observed during a period when only standard precautions are implemented, discontinuing contact precautions for patients carrying ESBL-producing Enterobacteriaceae.

Regular assessments during hospital stay up to 6 months

Evaluation at Discharge

Duration - Single day at discharge

Participants complete self-questionnaires evaluating satisfaction and mental health on the day of discharge, typically around day 11 of their hospital stay.

1 visit (in-person) on discharge day

Trial Site Locations

Total: 1 location

1

CHR Metz-Thionville/Hôpital Bel Air

Metz, France, 57085

Actively Recruiting

Loading map...

Research Team

L

Laurie RENAUDIN, MD

M

Mathieu LLORENS, MD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

PREVENTION

Number of Arms

2

Similar Trials

Hydrogen Peroxide and Ultraviolet Light for Disinfecting Sur...

Infection, Hospital

Actively Recruiting

12 locations

Infectious Complications After Cystectomy: A Prospective Obs...

Bladder Cancer

Actively Recruiting

1 location

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here