Status:

UNKNOWN

A Study to Investigate the Transmission and Burden of PVL-MRSA in Households in Sri Lanka

Lead Sponsor:

University of Sheffield

Collaborating Sponsors:

Rajarata University, Sri Lanka

Conditions:

Staphylococcus Aureus

Eligibility:

All Genders

18+ years

Brief Summary

This study will determine the frequency of Staphylococcus aureus carriage in household contacts of individuals with clinical infection due to this pathogen. It will also assess the frequency of transm...

Detailed Description

This is a prospective cohort study based at Anuradhapura Teaching Hospital (Sri Lanka). Potential index study participants will have clinical infection caused by Staphylococcus aureus and will be iden...

Eligibility Criteria

Inclusion

  • Inclusion Criteria (index patient):
  • Confirmed clinical infection caused by Staphylococcus aureus infection, including skin and soft tissue infection (SSTI) or infection of a normally sterile site.
  • Participant is willing and able to give informed consent for participation in the study.
  • Male or Female greater or equal to 18 years old.
  • Household is within one day's travel of the Hospital.
  • Inclusion Criteria (household contact):
  • Resident in the same household as index participant.
  • Participant is willing and able to give informed consent for participation in the study if greater or equal to 18 years old or the parent/legal guardian if participant is less than 18 years old.
  • Likely continued household residence for at least 3 months from initial sample collection.
  • Able to comply with study requirements.
  • Exclusion Criteria (index patient):
  • \- Deemed unsuitable by the responsible clinical team/clinician (e.g. terminal illness).
  • Exclusion Criteria (household contact):
  • Not a resident of the household at the time of the index patient hospital admission.
  • Deemed unsuitable by the responsible clinical team/clinician (e.g. terminal illness)
  • At least 4 household contacts already enrolled to this study.

Exclusion

    Key Trial Info

    Start Date :

    May 1 2021

    Trial Type :

    OBSERVATIONAL

    Allocation :

    ESTIMATED

    End Date :

    September 1 2021

    Estimated Enrollment :

    300 Patients enrolled

    Trial Details

    Trial ID

    NCT04884958

    Start Date

    May 1 2021

    End Date

    September 1 2021

    Last Update

    May 13 2021

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