Tracing MRSA in Households With Patients Infected With CA-MRSA by WGS
NCT ID: NCT04312776
Last Updated: 2020-03-18
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
10 participants
OBSERVATIONAL
2019-11-15
2020-03-17
Brief Summary
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Detailed Description
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1. Inclusion criteria: Patients (Child, Adult) with infections caused by S. aureus from the sites as follows: blood stream, skin or soft tissue, cerebrospinal fluid, bone and joint, genitourinary tract, infection of indwelling intravascular device, surgical wound, respiratory tract (organism grown from sputum and infiltrate on chest X-ray), peritoneal fluid or other otherwise sterile body fluids.
2. Exclusion criteria: Patients with risk factors for nosocomial or medically related infections, and patients who have been decolonized (using mupirocin, chlorhexidine or bleach) in the past month.
Outcome measures:
1. Isolation rate of staphylococcus aureus and methicillin-resistant staphylococcus aureus on domestic environment, contact and pets and livestock.
2. Molecular characteristics of CA-MRSA isolates recovered in Chinese hospitals, home environments, contacts, and pets and livestock.
Definition:
A MRSA infection was considered to be HA-MRSA by the CDC epidemiologic definitions if, in the year prior to culture, the subject had surgery, hospitalization, hemodialysis or a stay in a long-term care facility, if an indwelling vascular catheter was in place at the time of culture, or if the subject was an inpatient hospitalized for 2 days at the time of culture. Otherwise, the subject was considered to have a CA-MRSA infection.
Conditions
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Study Design
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FAMILY_BASED
PROSPECTIVE
Study Groups
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Patients infected with CA-MRSA
It is an observational study, no interventions to any of the two study arms.
none intervention
Healthy people without any infection
It is an observational study, no interventions to any of the two study arms.
none intervention
Interventions
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none intervention
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
21 Years
70 Years
ALL
Yes
Sponsors
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Sir Run Run Shaw Hospital
OTHER
Responsible Party
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Jian-cang Zhou M.D.
Prof.
Principal Investigators
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Yun-song Yu, MD
Role: PRINCIPAL_INVESTIGATOR
Sir Run Run Shaw Hospital
Locations
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Sir Run Run Shaw Hospital
Hanzhou, Zhejiang, China
Countries
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Other Identifiers
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SRRSH-Household01
Identifier Type: -
Identifier Source: org_study_id
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