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Comparison · NCT02619994-df8dc032

Experimental Arm vs Control Arm: Treatment Success According to Pyrazinamide Resistance (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. Experimental Arm vs Control Arm: Treatment Success According to Pyrazinamide Resistance (2). Trial comparisons, record NCT02619994-df8dc032. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02619994-df8dc032

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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 10.7620.6150.865wilson
Risk in group 20.7880.660.878wilson
Risk difference, group 1 minus group 2-0.0266-0.1990.139newcombe hybrid score
Risk ratio, group 1 over group 20.9660.7751.2log
Odds ratio, group 1 over group 20.8590.3242.27log
Number needed to treat, for one fewer participant with the outcome on Experimental Arm than on Control Arm37.7from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: control.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Experimental Arm
Regimen consists of only oral medication using delamanid, linezolid, levofloxacin, and pyrazinamide, for nine or twelve months depending on the time of sputum culture conversion to negative.~* Delamanid (100 mg bid for the entire treatment period)~* Linezolid (600mg/day for 2 months and 300mg/day afterwards until the end of treatment)~* Levofloxacin (750 \~1000 mg/day)~* Pyrazinamide (1000\~ 2000 mg/day)~Linezolid~Delamanid~Levofloxacin~Pyrazinamide
3242OG001
Group 2Control Arm
Regimen is the locally-used WHO-approved MDR-TB regimen in Korea based on 2014 Korean guideline of TB management.~* Intensive phase regimen consists of four effective second-line anti-TB drugs (including injectables) and pyrazinamide.~* Treatment duration: for at least 20 months~Locally-used WHO-approved MDR-TB regimen in Korea
4152OG000

Outcome

Type
SECONDARY
Title
Treatment Success According to Pyrazinamide Resistance (2)
Description
Treatment success rate of participants without pyrazinamide resistance in the mITT analysis
Time frame
At 24 months after treatment start
Population
mITT population Participant with \[not assessable\] was not included in the analysis

Source ClinicalTrials.gov

Trial

Title
Treatment Shortening of MDR-TB Using Existing and New Drugs
NCT number
NCT02619994
Phases
PHASE2
Conditions
Tuberculosis, Multidrug-Resistant
Interventions
Linezolid, Delamanid, Levofloxacin, Pyrazinamide, Locally-used WHO-approved MDR-TB regimen in Korea
Lead sponsor
Seoul National University Hospital
Results first posted
2025-01-03

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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