Comparison · NCT00955487-b59c753f
Inhaled Nitric Oxide (iNO) vs Placebo (Nitrogen): Sepsis
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. Inhaled Nitric Oxide (iNO) vs Placebo (Nitrogen): Sepsis. Trial comparisons, record NCT00955487-b59c753f. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00955487-b59c753f
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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 | 0.22 | 0.134 | 0.341 | wilson | |
| Risk in group 2 | 0.215 | 0.133 | 0.33 | wilson | |
| Risk difference, group 1 minus group 2 | 0.00495 | -0.139 | 0.151 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 1.02 | 0.525 | 1.99 | log | |
| Odds ratio, group 1 over group 2 | 1.03 | 0.438 | 2.42 | log | |
| Number needed to treat, for one more participant with the outcome on Inhaled Nitric Oxide (iNO) than on Placebo (Nitrogen) | 202 | from the risk difference interval | the interval includes no difference |
Source ClinicalTrials.gov
Groups2
Group 2 names the comparator: placebo.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | Inhaled Nitric Oxide (iNO) | Participants will receive a low concentration of iNO until they are 30 weeks corrected gestational age or for 14 days if they were born at 29 weeks or more.~Inhaled Nitric Oxide (iNO) will be delivered using the iNOVent device to provide 10 ppm proximally (yielding approximately 5 ppm to the posterior pharynx). | 13 | 59 | OG000 |
| Group 2 | Placebo (Nitrogen) | Participants will receive Placebo until they are 30 weeks corrected gestational age or for 14 days if they were born at 29 weeks or more.~Placebo will be delivered using the iNOVent device to provide 10 ppm proximally (yielding approximately 5 ppm to the posterior pharynx). | 14 | 65 | OG001 |
Source ClinicalTrials.gov
Outcome
- Type
- SECONDARY
- Title
- Sepsis
- Description
- Number of participants that developed sepsis
- Time frame
- Randomization to discharge
- Population
Source ClinicalTrials.gov
Trial
- Title
- Examining the Use of Non-Invasive Inhaled Nitric Oxide to Reduce Chronic Lung Disease in Premature Newborns
- NCT number
- NCT00955487
- Phases
- PHASE2
- Conditions
- Bronchopulmonary Dysplasia
- Interventions
- Inhaled Nitric Oxide (iNO), Nitrogen (placebo)
- Lead sponsor
- University of Colorado, Denver
- Results first posted
- 2017-05-23
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT00955487?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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