Comparison · NCT00819052-sae
Nevirapine Immediate Release (NVP IR) vs Nevirapine Extended Release (NVP XR): serious adverse events
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. Nevirapine Immediate Release (NVP IR) vs Nevirapine Extended Release (NVP XR): serious adverse events. Trial comparisons, record NCT00819052-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00819052-sae
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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 | 0.223 | 0.163 | 0.297 | wilson | |
| Risk in group 2 | 0.247 | 0.202 | 0.3 | wilson | |
| Risk difference, group 1 minus group 2 | -0.0245 | -0.104 | 0.0622 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 0.901 | 0.628 | 1.29 | log | |
| Odds ratio, group 1 over group 2 | 0.873 | 0.546 | 1.39 | log | |
| Number needed to treat, for one fewer participant with a serious adverse event on Nevirapine Immediate Release (NVP IR) than on Nevirapine Extended Release (NVP XR) | 40.8 | from the risk difference interval | the interval includes no difference |
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 | Nevirapine Immediate Release (NVP IR) | Nevirapine immediate release 200 mg tablets given twice daily | 33 | 148 | EG000 |
| Group 2 | Nevirapine Extended Release (NVP XR) | Nevirapine extended release 400 mg tablets given once daily | 73 | 295 | EG001 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
- 144 weeks
Source ClinicalTrials.gov
Trial
- Title
- Switching Nevirapine Immediate Release( IR) Based Regimen to Nevirapine Extended Release (XR) Based Regimen in Human Immunodeficiency Virus One (HIV-1) Infected Patients
- NCT number
- NCT00819052
- Phases
- PHASE3
- Conditions
- HIV Infections
- Interventions
- Nevirapine XR, Nevirapine XR, Nevirapine IR
- Lead sponsor
- Boehringer Ingelheim
- Results first posted
- 2012-02-24
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT00819052?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.
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