Comparison · NCT01635439-78ea41de
Propess vs Prostin E2: Uterine Hyper-stimulation Rate
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. Propess vs Prostin E2: Uterine Hyper-stimulation Rate. Trial comparisons, record NCT01635439-78ea41de. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01635439-78ea41de
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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 | 0.01 | 0.00177 | 0.0545 | wilson | |
| Risk in group 2 | 0.01 | 0.00177 | 0.0545 | wilson | |
| Risk difference, group 1 minus group 2 | 0 | -0.0452 | 0.0452 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 1 | 0.0634 | 15.8 | log | |
| Odds ratio, group 1 over group 2 | 1 | 0.0617 | 16.2 | log | |
| Number needed to treat | from the risk difference interval | the two groups' risks are equal |
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 | Propess | Propess insert is a preparation of PGE2 packaged in a hydrogel polymer matrix and designed for slow intravaginal release of 10 mg dinoprostone at a rate of 0.3 mg/h over 12 h. | 1 | 100 | OG000 |
| Group 2 | Prostin E2 | PROSTIN E2 Vaginal Suppository, an oxytocic, contains dinoprostone as the naturally occurring prostaglandin E2 (PGE2)3 mg/suppository. | 1 | 100 | OG001 |
Source ClinicalTrials.gov
Outcome
- Type
- SECONDARY
- Title
- Uterine Hyper-stimulation Rate
- Description
- Time frame
- 24 hours
- Population
Source ClinicalTrials.gov
Trial
- Title
- Prostin and Propess in Induction of Labor
- NCT number
- NCT01635439
- Phases
- PHASE3
- Conditions
- Labor Pain
- Interventions
- Propess, Prostin E2
- Lead sponsor
- Ain Shams University
- Results first posted
- 2012-10-04
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT01635439?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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