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Mastering Hospital Antimicrobial Resistance and Its Spread Into the Community

T

Tel Aviv Sourasky Medical Center

Status

Unknown

Conditions

Bacterial Infection

Study type

Observational

Funder types

Other

Identifiers

NCT00765778
TASMC-08-YC-249-CTIL

Details and patient eligibility

About

Detailed activity:

  • Family members and caregivers of carrier residents will be screened for ESBL and MRSA. Screening will be performed by obtaining nares and perirectal cultures. Nares cultures will be obtained by ward staff or research personnel who are experienced in performing this activity: a moisture swab will be applied gently to the distal part of both nares. Perirectal cultures, will be taken by swab, who will be applied to the perirectal area, either by staff as mentioned above, or will be given to the participants to perform by himself (with explanation on how to perform it).
  • The Family and Caregiver Screening Form will be filled out; results of screening will be added to the forms. This data will be stored after removal of all Family members' identifiers for further analysis.
  • In order to allow follow up, a list linking between the Family members' study number and his identifying details will be kept separately in the rehabilitation center. This list will not be transferred elsewhere.

Full description

Detailed activity:

  • Family members and caregivers of carrier residents will be screened for ESBL and MRSA. Screening will be performed by obtaining nares and perirectal cultures. Nares cultures will be obtained by ward staff or research personnel who are experienced in performing this activity: a moisture swab will be applied gently to the distal part of both nares. Perirectal cultures, will be taken by swab, who will be applied to the perirectal area, either by staff as mentioned above, or will be given to the participants to perform by himself (with explanation on how to perform it).
  • The Family and Caregiver Screening Form will be filled out; results of screening will be added to the forms. This data will be stored after removal of all Family members' identifiers for further analysis.
  • In order to allow follow up, a list linking between the Family members' study number and his identifying details will be kept separately in the rehabilitation center. This list will not be transferred elsewhere.
  • Providing results to family members: results of screening will be / will not be reported to the participant (family member) based on local decision in each center.

Enrollment

400 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Family members or caregivers of patient hospitalized in rehabilitation center and who is known carrier of the target resistant population.
  • Participating member older than 18 years, who attend the patient at least once a week, will be eligible for inclusion.

Exclusion criteria

  • Age 18 years or less, attending the patient less than once a week.

Trial contacts and locations

1

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Central trial contact

yaffa lerman, MD

Data sourced from clinicaltrials.gov

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