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Comparison · NCT00867048-80175d7f

Early ART vs Deferred ART: Transmission Risk Behavior Outcome 2

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Early ART vs Deferred ART: Transmission Risk Behavior Outcome 2. Trial comparisons, record NCT00867048-80175d7f. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00867048-80175d7f

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.1080.08980.13wilson
Risk in group 20.0830.06720.102wilson
Risk difference, group 1 minus group 20.0251-0.001340.0519newcombe hybrid score
Risk ratio, group 1 over group 21.30.9861.72log
Odds ratio, group 1 over group 21.340.9841.82log
Number needed to treat, for one more participant with the outcome on Early ART than on Deferred ART39.8from the risk difference intervalthe interval includes no difference

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Early ART
Initiate ART immediately following randomization~All licensed antiretroviral medications: In both arms, participants may be prescribed any licensed antiretroviral medication, in accordance with national treatment guidelines. The nature of the intervention is the timing of when to begin treatment with these medications, as described in the two treatment arms.~ART dosage and frequency were based on clinical decision in accordance with local/national prescribing guidelines.
101934OG000
Group 2Deferred ART
Defer ART until the CD4+ count declines to \<350 cells/cu mm or AIDS develops~All licensed antiretroviral medications: In both arms, participants may be prescribed any licensed antiretroviral medication, in accordance with national treatment guidelines. The nature of the intervention is the timing of when to begin treatment with these medications, as described in the two treatment arms.~ART dosage and frequency were based on clinical decision in accordance with local/national prescribing guidelines.
80964OG001

Outcome

Type
SECONDARY
Title
Transmission Risk Behavior Outcome 2
Description
Percentage of participants identifying as hetrosexual engaging in condomless sex with HIV serodifferent partners (CLS-D) at study month 12. Participant completed a self-reported questionnaire on transmission risk behavior during the past two months at the month 12 visit following randomization.
Time frame
12 month visit
Population

Source ClinicalTrials.gov

Trial

Title
Strategic Timing of Antiretroviral Treatment
NCT number
NCT00867048
Phases
PHASE4
Conditions
HIV Infection
Interventions
All licensed antiretroviral medications
Lead sponsor
University of Minnesota
Results first posted
2023-12-20

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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