Comparison · NCT00630812-sae
Mannitol 400mg vs Control: 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. Mannitol 400mg vs Control: serious adverse events. Trial comparisons, record NCT00630812-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00630812-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 | 0.168 | 0.121 | 0.229 | wilson | |
| Risk in group 2 | 0.248 | 0.18 | 0.332 | wilson | |
| Risk difference, group 1 minus group 2 | -0.0795 | -0.176 | 0.012 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 0.68 | 0.435 | 1.06 | log | |
| Odds ratio, group 1 over group 2 | 0.615 | 0.349 | 1.08 | log | |
| Number needed to treat, for one fewer participant with a serious adverse event on Mannitol 400mg than on Control | 12.6 | from the risk difference interval | the interval includes no difference |
Source ClinicalTrials.gov
Groups2
Group 2 names the comparator: control.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | Mannitol 400mg | active treatment~inhaled mannitol: 400 mg BD for 26 + 26 weeks | 31 | 184 | EG000 |
| Group 2 | Control | Control (40mg inhaled mannitol) : BD for 26 weeks followed by 26 weeks of inhaled mannitol in the open label phase | 30 | 121 | EG001 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
- 26 weeks
Source ClinicalTrials.gov
Trial
- Title
- Long Term Administration of Inhaled Mannitol in Cystic Fibrosis
- NCT number
- NCT00630812
- Phases
- PHASE3
- Conditions
- Cystic Fibrosis
- Interventions
- inhaled mannitol, Placebo comparator
- Lead sponsor
- Syntara
- Results first posted
- 2020-10-09
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT00630812?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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GET https://conductscience.org/api/comparisons/v1/NCT00630812-sae