Comparison · NCT00827983-sae
Progesterone SC vs Progesterone Vaginal Gel: 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. Progesterone SC vs Progesterone Vaginal Gel: serious adverse events. Trial comparisons, record NCT00827983-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00827983-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 | 0.0414 | 0.0248 | 0.0683 | wilson | |
| Risk in group 2 | 0.0581 | 0.0379 | 0.0881 | wilson | |
| Risk difference, group 1 minus group 2 | -0.0167 | -0.051 | 0.0169 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 0.712 | 0.366 | 1.39 | log | |
| Odds ratio, group 1 over group 2 | 0.7 | 0.348 | 1.41 | log | |
| Number needed to treat, for one fewer participant with a serious adverse event on Progesterone SC than on Progesterone Vaginal Gel | 59.8 | 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 | Progesterone SC | Progesterone SC was administered at a daily dosage of 25 mg during a minimum of two weeks (in case of no pregnancy) to a maximum of 10 weeks (in case of pregnancy) | 14 | 338 | EG000 |
| Group 2 | Progesterone Vaginal Gel | Progesterone Vaginal gel was administered at a daily dosage of 90 mg during a minimum of two weeks (in case of no pregnancy) to a maximum of 10 weeks (in case of pregnancy) | 20 | 344 | EG001 |
Source ClinicalTrials.gov
Harm
- What it counts
- Total, serious adverse events
- Time frame
- Adverse events were collected during the 10 weeks of treatment, with a follow-up period of 6 months
Source ClinicalTrials.gov
Trial
- Title
- Subcutaneous Progesterone Versus Vaginal Progesterone Gel for Luteal Phase Support in Patients Undergoing In-Vitro Fertilization (IVF)
- NCT number
- NCT00827983
- Phases
- PHASE3
- Conditions
- In Vitro Fertilization
- Interventions
- Progesterone, Progesterone
- Lead sponsor
- IBSA Institut Biochimique SA
- Results first posted
- 2012-12-26
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT00827983?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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