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Comparison · NCT00448669-511386a5

TDF-FTC, Condoms, Risk Counseling vs Placebo, Condoms, Risk Counseling: Antiretroviral (ARV) Resistance Patterns in Seroconverters

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. TDF-FTC, Condoms, Risk Counseling vs Placebo, Condoms, Risk Counseling: Antiretroviral (ARV) Resistance Patterns in Seroconverters. Trial comparisons, record NCT00448669-511386a5. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00448669-511386a5

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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 10.10.01790.404wilson
Risk in group 20.03850.006820.189wilson
Risk difference, group 1 minus group 20.0615-0.110.367newcombe hybrid score
Risk ratio, group 1 over group 22.60.17937.7log
Odds ratio, group 1 over group 22.780.15749.2log
Number needed to treat, for one more participant with the outcome on TDF-FTC, Condoms, Risk Counseling than on Placebo, Condoms, Risk Counseling16.3from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1TDF-FTC, Condoms, Risk Counseling
Participants randomized to the active arm received daily oral TDF-FTC along with male and female condoms, personalized risk reduction counseling, adherence counseling, and routine monitoring for HIV infection, laboratory abnormalities, and adverse events.~Tenofovir Disoproxil Fumarate 300 mg + Emtricitabine 200 mg: Daily oral single dose pill containing 300 mg TDF and 200 mg FTC.
110OG000
Group 2Placebo, Condoms, Risk Counseling
Participants randomized to the placebo arm received a daily oral placebo tablet along with male and female condoms, personalized risk reduction counseling, adherence counseling, and routine monitoring for HIV infection, laboratory abnormalities, and adverse events.~TDF-FTC placebo: Placebo comparator for TDF-FTC
126OG001

Outcome

Type
SECONDARY
Title
Antiretroviral (ARV) Resistance Patterns in Seroconverters
Description
Participants who seroconverted had blood samples taken at the time of infection and at one month and six months post seroconversion to detect any HIV resistance mutations.
Time frame
At time HIV infection diagnosed,1 month post-time of HIV infection diagnosis, and 6 months post-time of HIV infection diagnosis
Population

Source ClinicalTrials.gov

Trial

Title
Botswana TDF/FTC Oral HIV Prophylaxis Trial
NCT number
NCT00448669
Phases
PHASE2, PHASE3
Conditions
HIV Infections
Interventions
Tenofovir Disoproxil Fumarate 300 mg + Emtricitabine 200 mg, Placebo Oral Tablet
Lead sponsor
Centers for Disease Control and Prevention
Results first posted
2020-02-05

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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