Comparison · NCT01222247-c45a693f
Betamethasone vs Placebo: Number of Neonates With Transient Tachypnea of the Newborn
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. Betamethasone vs Placebo: Number of Neonates With Transient Tachypnea of the Newborn. Trial comparisons, record NCT01222247-c45a693f. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01222247-c45a693f
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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 | 0.0666 | 0.0548 | 0.0807 | wilson | |
| Risk in group 2 | 0.0986 | 0.084 | 0.115 | wilson | |
| Risk difference, group 1 minus group 2 | -0.032 | -0.0525 | -0.0117 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 0.675 | 0.526 | 0.868 | log | |
| Odds ratio, group 1 over group 2 | 0.652 | 0.497 | 0.856 | log | |
| Number needed to treat, for one fewer participant with the outcome on Betamethasone than on Placebo | 31.3 | 19.1 | 85.3 | from the risk difference interval |
Source ClinicalTrials.gov
Groups2
Group 2 names the comparator: placebo.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | Betamethasone | A course of two 2mL intramuscular (IM) injections containing 3 mg of betamethasone, 24 hours apart | 95 | 1,427 | OG000 |
| Group 2 | Placebo | A similar course of an identical appearing placebo: two 2 mL IM injections of placebo, 24 hours apart~Placebo: Similar course of identical appearing placebo: 2 mL IM injections, 24 hours apart. | 138 | 1,400 | OG001 |
Source ClinicalTrials.gov
Outcome
- Type
- SECONDARY
- Title
- Number of Neonates With Transient Tachypnea of the Newborn
- Description
TTN is defined as signs of respiratory distress, specifically tachypnea, that are resolved by 72 hours of age. TTN may be diagnosed in the absence of a chest X-ray or with a chest X-ray that is normal or shows signs of increased perihilar interstitial markings
- Time frame
- by 72 hours after delivery
- Population
- The number of participants analyzed accounts for the 4 participants for which baseline measures were obtained but who were subsequently lost to follow-up (2 in each group).
Source ClinicalTrials.gov
Trial
- Title
- Antenatal Late Preterm Steroids (ALPS): A Randomized Placebo-Controlled Trial
- NCT number
- NCT01222247
- Phases
- PHASE3
- Conditions
- Pregnancy, Respiratory Distress Syndrome, Pregnancy Outcomes, Preterm Birth
- Interventions
- Betamethasone, Placebo
- Lead sponsor
- The George Washington University Biostatistics Center
- Results first posted
- 2019-01-30
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT01222247?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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