Comparison · NCT03089983-dca45754
Standard Isoniazid (INH) for 26 Weeks vs Short-course Isoniazid + Rifapentine (INH + RIF) for 12 Weeks: Discontinuation Due to Experiencing an Adverse Event
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
2 sourcestrial-comparisons-2026-03-23-0.1.0
Cite this record
ConductScience Library. Standard Isoniazid (INH) for 26 Weeks vs Short-course Isoniazid + Rifapentine (INH + RIF) for 12 Weeks: Discontinuation Due to Experiencing an Adverse Event. Trial comparisons, record NCT03089983-dca45754. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03089983-dca45754
On this page
Measures6
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
| Measure | Value | 95% interval, lower | 95% interval, upper | Method | Note |
|---|---|---|---|---|---|
| Risk in group 1 | 0.0641 | 0.0352 | 0.114 | wilson | |
| Risk in group 2 | 0.00641 | 0.00113 | 0.0354 | wilson | |
| Risk difference, group 1 minus group 2 | 0.0577 | 0.0167 | 0.108 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 10 | 1.3 | 77.2 | log | |
| Odds ratio, group 1 over group 2 | 10.6 | 1.34 | 84 | log | |
| Number needed to treat, for one more participant with the outcome on Standard Isoniazid (INH) for 26 Weeks than on Short-course Isoniazid + Rifapentine (INH + RIF) for 12 Weeks | 17.3 | 9.27 | 59.7 | from the risk difference interval |
Source ClinicalTrials.gov
Groups2
Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | Standard Isoniazid (INH) for 26 Weeks | Participants will be randomized to receive INH, the standard of care in Malaysia, for 26 weeks while in prison as TB preventative treatment | 10 | 156 | OG000 |
| Group 2 | Short-course Isoniazid + Rifapentine (INH + RIF) for 12 Weeks | Participants will be randomized to receive INH + RIF as TB preventative treatment for 12 weeks while in prison. | 1 | 156 | OG001 |
Source ClinicalTrials.gov
Outcome
- Type
- SECONDARY
- Title
- Discontinuation Due to Experiencing an Adverse Event
- Description
- The number of participants that discontinued the trial due to experiencing an Adverse Event
- Time frame
- up to 6 months
- Population
Source ClinicalTrials.gov
Trial
- Title
- Addiction, HIV and Tuberculosis in Malaysian Criminal Justice Settings
- NCT number
- NCT03089983
- Phases
- NA
- Conditions
- Opioid Dependence, Addiction, HIV/AIDS, Tuberculosis, Hepatitis
- Interventions
- Isoniazid, Rifapentine
- Lead sponsor
- Yale University
- Results first posted
- 2026-02-09
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT03089983?tab=results
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.
For software
Read this comparison from software.
The record is JSON. No key.
GET https://conductscience.org/api/comparisons/v1/NCT03089983-dca45754