Comparison · NCT01850030-sae
Dydrogesterone 30 mg vs Micronized Progesterone 600 mg: 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. Dydrogesterone 30 mg vs Micronized Progesterone 600 mg: serious adverse events. Trial comparisons, record NCT01850030-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01850030-sae
On this page
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 | 0.108 | 0.0842 | 0.138 | wilson | |
| Risk in group 2 | 0.133 | 0.106 | 0.165 | wilson | |
| Risk difference, group 1 minus group 2 | -0.025 | -0.0651 | 0.015 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 0.812 | 0.583 | 1.13 | log | |
| Odds ratio, group 1 over group 2 | 0.79 | 0.542 | 1.15 | log | |
| Number needed to treat, for one fewer participant with a serious adverse event on Dydrogesterone 30 mg than on Micronized Progesterone 600 mg | 40.1 | from the risk difference interval | the interval includes no difference |
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 | Dydrogesterone 30 mg | Dydrogesterone 30 mg: Oral Dydrogesterone 10 mg tablets tid~Placebo progesterone: Placebo intravaginal micronized progesterone 200 mg capsules tid | 56 | 518 | EG000 |
| Group 2 | Micronized Progesterone 600 mg | Micronized Progesterone 600 mg: Intravaginal micronized progesterone 200 mg capsules tid~Placebo dydrogesterone: placebo oral dydrogesterone 10 mg tablets tid | 68 | 511 | EG001 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
Source ClinicalTrials.gov
Trial
- Title
A Multicenter Study Comparing the Efficacy, Safety and Tolerability of Oral Dydrogesterone 30 mg Daily Versus Intravaginal Micronized Progesterone Capsules 600 mg Daily for Luteal Support in In-Vitro Fertilization
- NCT number
- NCT01850030
- Phases
- PHASE3
- Conditions
- Female Infertility
- Interventions
- Dydrogesterone 30 mg, Micronized Progesterone 600 mg, Placebo progesterone, Placebo dydrogesterone
- Lead sponsor
- Abbott
- Results first posted
- 2018-01-02
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT01850030?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.
For software
Read this comparison from software.
The record is JSON. No key.
GET https://conductscience.org/api/comparisons/v1/NCT01850030-sae