ConductScience.org, home

Comparison · NCT00147199-sae

Inhaled Treprostinil vs Placebo: serious adverse events

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

Download JSON
Cite this record

ConductScience Library. Inhaled Treprostinil vs Placebo: serious adverse events. Trial comparisons, record NCT00147199-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00147199-sae

On this page

Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.07830.04170.142wilson
Risk in group 20.1080.06440.177wilson
Risk difference, group 1 minus group 2-0.0301-0.1070.0474newcombe hybrid score
Risk ratio, group 1 over group 20.7220.3211.62log
Odds ratio, group 1 over group 20.6990.2871.7log
Number needed to treat, for one fewer participant with a serious adverse event on Inhaled Treprostinil than on Placebo33.3from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Inhaled TreprostinilInitial dose: 3 breaths. Titrated to 9 breaths, four times daily.9115EG000
Group 2PlaceboIdentical placebo inhalation solution13120EG001

Harm

What it counts
Total, serious adverse events
Time frame
12 Weeks

Source ClinicalTrials.gov

Trial

Title
Clinical Investigation Into Inhaled Treprostinil Sodium in Patients With Severe Pulmonary Arterial Hypertension (PAH)
NCT number
NCT00147199
Phases
PHASE3
Conditions
Pulmonary Hypertension
Interventions
Inhaled treprostinil, Placebo inhalation solution
Lead sponsor
United Therapeutics
Results first posted
2013-08-12

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/NCT00147199-sae