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Immediate Versus Deferred Start of Anti-HIV Therapy in HIV-Infected Adults Being Treated for Tuberculosis (STRIDE)

This study has been completed.
Sponsor:
Collaborator:
National Institute of Allergy and Infectious Diseases (NIAID)
Information provided by (Responsible Party):
AIDS Clinical Trials Group
ClinicalTrials.gov Identifier:
NCT00108862
First received: April 19, 2005
Last updated: July 9, 2012
Last verified: July 2012
History of Changes
Results First Received: September 27, 2011  
Study Type: Interventional
Study Design: Allocation: Randomized;   Endpoint Classification: Safety/Efficacy Study;   Intervention Model: Parallel Assignment;   Masking: Open Label;   Primary Purpose: Treatment
Conditions: HIV Infection
Tuberculosis
Interventions: Other: Strategy: Immediate ART
Other: Strategy: Deferred ART

  Participant Flow
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  Baseline Characteristics
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Reporting Groups
  Description
Immediate ART These participants initiated HIV antiretroviral therapy (ART) within 72 hours of randomization, which took place at most 2 weeks after initiating rifampin (RIF)- or other rifamycin-based TB treatment according to in-country national TB treatment guidelines. The study-provided drugs were efavirenz (EFV) 600 mg (provided to non-U.S. sites only; 1 tablet orally) and emtricitabine (FTC) 200 mg/tenofovir disoproxil fumarate (TDF) 300 mg (1 fixed-dose combination tablet orally) once daily. FTC 200 mg (1 capsule) and TDF 300 mg (1 tablet) could be substituted for the fixed-dose combination tablet and was provided by the study. Participants who could not tolerate EFV could be offered nevirapine (NVP) 200 mg daily for 14 days, then 200 mg twice daily. Substitutions with other locally-available U.S. Food and Drug Administration (FDA)-approved or tentatively approved antiretrovirals (ARVs) that were compatible with TB therapy could be used at the discretion of the site investigator.
Deferred ART These participants deferred ART until 8 to 12 weeks after initiation of their RIF- or other rifamycin-based TB treatment according to in-country national TB treatment guidelines. The study-provided drugs were EFV 600 mg (provided to non-U.S. sites only; 1 tablet orally) and FTC 200 mg/TDF 300 mg (1 fixed-dose combination tablet orally) once daily. FTC 200 mg (1 capsule) and TDF 300 mg (1 tablet) could be substituted for the fixed-dose combination tablet and was provided by the study. Participants who could not tolerate EFV could be offered NVP 200 mg daily for 14 days, then 200 mg twice daily. Substitutions with other locally-available U.S. FDA-approved or tentatively approved ARVs that were compatible with TB therapy could be used at the discretion of the site investigator.
Total Total of all reporting groups

Baseline Measures
    Immediate ART     Deferred ART     Total  
Number of Participants  
[units: participants]
 		  405     401     806  
Age  
[units: participants]
 		     
<=18 years     0     2     2  
Between 18 and 65 years     403     398     801  
>=65 years     2     1     3  
Age  
[units: years]
Median ( Inter-Quartile Range ) 		  34  
  ( 29 to 40 )   		  34  
  ( 29 to 42 )   		  34  
  ( 29 to 41 )  
Gender  
[units: participants]
 		     
Female     139     166     305  
Male     266     235     501  
Region of Enrollment  
[units: participants]
 		     
South Africa     109     112     221  
Malawi     69     68     137  
Brazil     57     56     113  
Kenya     36     36     72  
Peru     23     25     48  
India     26     21     47  
Zambia     17     17     34  
Zimbabwe     16     17     33  
Uganda     15     14     29  
Botswana     13     15     28  
Haiti     12     8     20  
United States     9     10     19  
Thailand     3     2     5  
TB Diagnosis Level at Entry  
[units: participants]
 		     
Confirmed TB     193     181     374  
Probable TB     208     218     426  
Not TB     4     2     6  
Drug-Resistant TB Status at Entry  
[units: participants]
 		     
Rifampin (RIF) Resistant TB     1     0     1  
Isoniazid (INH) Resistant TB     3     5     8  
RIF and INH Resistant TB (Multi-Drug Resistant TB)     1     4     5  
RIF and INH Sensitive TB     400     392     792  
Time to ART Start from Start of TB Medications  
[units: days]
Median ( Inter-Quartile Range ) 		  10  
  ( 7 to 12 )   		  70  
  ( 66 to 75 )   		  14  
  ( 10 to 70 )  



  Outcome Measures
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1.  Primary:   Percent of Participants Who Survived Without AIDS Progression.   [ Time Frame: Through week 48 ]
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2.  Secondary:   Percent of Participants Reporting a Grade 3 or 4 Adverse Event or Laboratory Abnormality   [ Time Frame: Through week 48 ]
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3.  Secondary:   Time to First New AIDS-defining Illness or Death.   [ Time Frame: Through week 48 ]
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4.  Secondary:   Percent of Participants With Culture-confirmed Tuberculosis (TB) Who Survived Without AIDS Progression.   [ Time Frame: Through week 48 ]
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5.  Secondary:   Percent of Participants Who Interrupted or Discontinued at Least One Tuberculosis (TB) Medication Due to Toxicity.   [ Time Frame: Through week 48 ]
  Show Outcome Measure 5

6.  Secondary:   Percent of Participants With Confirmed or Probable Tuberculosis (TB) Whose TB Resolved, or Who Required TB Treatment Through the End of Follow-up, or Died, or Were Lost to Follow-up.   [ Time Frame: Through week 48 ]
  Show Outcome Measure 6

7.  Secondary:   Percent of Participants Whose CD4 Increased by at Least 100 Cells/mm^3 Between Baseline and Week 48.   [ Time Frame: Through week 48 ]
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8.  Secondary:   Percent of Participants With MTB IRIS.   [ Time Frame: Through week 48 ]
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9.  Secondary:   Percent of Participants With HIV IRIS.   [ Time Frame: Through week 48 ]
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10.  Secondary:   Percent of Participants Whose HIV Viral Load Was Less Than 400 Copies/mL at Week 48.   [ Time Frame: Through week 48 ]
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11.  Other Pre-specified:   Percent of Participants in the Less Than 50 Cells/mm^3 CD4 Stratum Who Survived Without AIDS Progression.   [ Time Frame: Through week 48 ]
  Show Outcome Measure 11

12.  Other Pre-specified:   Percent of Participants in the Greater Than or Equal to 50 Cells/mm^3 CD4 Stratum Who Survived Without AIDS Progression.   [ Time Frame: Through week 48 ]
  Show Outcome Measure 12


  Serious Adverse Events
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  Other Adverse Events
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  More Information
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Certain Agreements:  
Principal Investigators are NOT employed by the organization sponsoring the study.
There IS an agreement between Principal Investigators and the Sponsor (or its agents) that restricts the PI's rights to discuss or publish trial results after the trial is completed.
The agreement is:
unchecked The only disclosure restriction on the PI is that the sponsor can review results communications prior to public release and can embargo communications regarding trial results for a period that is less than or equal to 60 days. The sponsor cannot require changes to the communication and cannot extend the embargo.
unchecked The only disclosure restriction on the PI is that the sponsor can review results communications prior to public release and can embargo communications regarding trial results for a period that is more than 60 days but less than or equal to 180 days. The sponsor cannot require changes to the communication and cannot extend the embargo.


Limitations and Caveats
Limitations of the study, such as early termination leading to small numbers of participants analyzed and technical problems with measurement leading to unreliable or uninterpretable data
None.  


Results Point of Contact:  
Name/Title: ClinicalTrials.gov Coordinator
Organization: Center for Biostatistics in AIDS Research, Harvard School of Public Health
phone: (617)432-2829
e-mail: CBAR.ClinicalTrials.Gov@sdac.harvard.edu


No publications provided by AIDS Clinical Trials Group

Publications automatically indexed to this study:


Responsible Party: AIDS Clinical Trials Group
ClinicalTrials.gov Identifier: NCT00108862     History of Changes
Other Study ID Numbers: ACTG A5221, 1U01AI068636, ACTG A5221
Study First Received: April 19, 2005
Results First Received: September 27, 2011
Last Updated: July 9, 2012
Health Authority: United States: Federal Government