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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 21 November 2016
Main ID:  NCT02175849
Date of registration: 25/06/2014
Prospective Registration: No
Primary sponsor: Oxford University Clinical Research Unit, Vietnam
Public title: Intensifying Multi-Drug Resistant Tuberculosis Contact Tracing by Social Network Analysis SNAP
Scientific title: Contact Tracing by Social Network Analysis to Enhance Multi-Drug Resistant Tuberculosis Case Finding in Hanoi, Vietnam
Date of first enrolment: December 2013
Target sample size: 596
Recruitment status: Completed
URL:  https://clinicaltrials.gov/show/NCT02175849
Study type:  Observational
Study design:  Observational Model: Cohort, Time Perspective: Prospective  
Phase:  N/A
Countries of recruitment
Vietnam
Contacts
Name:     Heiman F Wertheim, PhD
Address: 
Telephone:
Email:
Affiliation:  Oxford University Clinical Research Unit - Hanoi
Key inclusion & exclusion criteria

Inclusion Criteria:

- PATIENTS: Newly detected rifampicin resistant TB or MDR-TB patients living in Hanoi
for at least 3 months preceding a diagnosis made between 2013-2015.

- CONTACTS: During the 3 months before the patient's TB or MDR-TB diagnosis: all
persons who spend an average of >4 hours per day in the same residence as the patient
AND/OR any individual who has had frequent and prolonged contact with the patient
AND/OR anyone who has spent time in a closed environment with an MDR-TB patient

- PATIENTS AND CONTACTS: All ages

- PATIENTS AND CONTACTS: Living in Hanoi during the study period.

Exclusion Criteria:

-PATIENTS AND CONTACTS: Lack of informed consent for participation.



Age minimum: N/A
Age maximum: N/A
Gender: Both
Health Condition(s) or Problem(s) studied
Tuberculosis Infection
Intervention(s)
Primary Outcome(s)
Yield of MDR-TB case detection through SNA [Time Frame: Six months]
Secondary Outcome(s)
MDR-TB incidence among subgroups of contacts [Time Frame: Six months]
Cost-effectiveness ratio of SNA and passive case finding strategies [Time Frame: Six months]
MDR-TB incidence among rifampicin resistant TB cases [Time Frame: Six months]
MDR-TB genotype [Time Frame: Six months]
Secondary ID(s)
10TB
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
National Tuberculosis Program, Vietnam
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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