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Prevalence of HIV and Tuberculosis in Masiphumelele Township, Cape Town, South Africa

This study has been completed.
Sponsor:
Collaborator:
National Institute of Allergy and Infectious Diseases (NIAID)
Information provided by:
CIPRA SA
ClinicalTrials.gov Identifier:
NCT00096681
First received: November 12, 2004
Last updated: February 17, 2011
Last verified: February 2011
History of Changes
Results First Received: January 14, 2011  
Study Type: Observational
Study Design: Observational Model: Ecologic or Community;   Time Perspective: Prospective
Conditions: HIV Infections
Tuberculosis

  Participant Flow
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Recruitment Details
Key information relevant to the recruitment process for the overall study, such as dates of the recruitment period and locations
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Pre-Assignment Details
Significant events and approaches for the overall study following participant enrollment, but prior to group assignment
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Reporting Groups
  Description
Participants From the Community The number of participants from the community who attended the clinic for a once off study visit

Participant Flow:   Overall Study
    Participants From the Community  
STARTED     762  
COMPLETED     762  
NOT COMPLETED     0  



  Baseline Characteristics
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Reporting Groups
  Description
Participants From the Community The number of participants from the community who attended the clinic for a once off study visit

Baseline Measures
    Participants From the Community  
Number of Participants  
[units: participants]
 		  762  
Age  
[units: participants]
 		 
<=18 years     26  
Between 18 and 65 years     726  
>=65 years     10  
Age  
[units: years]
Mean ± Standard Deviation 		  30  ± 11.1  
Gender  
[units: participants]
 		 
Female     422  
Male     340  
Region of Enrollment  
[units: participants]
 		 
South Africa     762  



  Outcome Measures
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1.  Primary:   Number of Participants With Microbiologically Confirmed Pulmonary Tuberculosis   [ Time Frame: Pulmonary Tuberculosis diagnosed from sputum sample obtained at the study visit ]
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2.  Secondary:   Number of Participants With a Positive HIV Test   [ Time Frame: HIV status at the time of the study visit ]
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  Serious Adverse Events
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  Other Adverse Events
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  More Information
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