Comparison · NCT00719186-05e3000b
Arm A: Clomiphene Citrate vs Arm B: Letrozole: Live Birth
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. Arm A: Clomiphene Citrate vs Arm B: Letrozole: Live Birth. Trial comparisons, record NCT00719186-05e3000b. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00719186-05e3000b
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 | 0.191 | 0.155 | 0.234 | wilson | |
| Risk in group 2 | 0.275 | 0.233 | 0.323 | wilson | |
| Risk difference, group 1 minus group 2 | -0.0839 | -0.144 | -0.0234 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 0.695 | 0.534 | 0.906 | log | |
| Odds ratio, group 1 over group 2 | 0.623 | 0.442 | 0.878 | log | |
| Number needed to treat, for one fewer participant with the outcome on Arm A: Clomiphene Citrate than on Arm B: Letrozole | 11.9 | 6.96 | 42.8 | from the risk difference interval |
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 | Arm A: Clomiphene Citrate | Clomiphene citrate 50 mg every day for 5 days (day 3-7 of cycle), for a total of 5 cycles or 20 weeks~Clomiphene citrate: Clomiphene citrate 50 mg every day for 5 days (day 3-7 of cycle), for a total of 5 cycles or 20 weeks | 72 | 376 | OG000 |
| Group 2 | Arm B: Letrozole | Letrozole 2.5 mg every day for 5 days (day 3-7 of cycle), for a total of 5 cycles or 20 weeks~Letrozole: Letrozole 2.5 mg every day for 5 days (day 3-7 of cycle), for a total of 5 cycles or 20 weeks | 103 | 374 | OG001 |
Source ClinicalTrials.gov
Outcome
- Type
- PRIMARY
- Title
- Live Birth
- Description
- The primary outcome measure is the occurrence of a live birth during the study period. Safety measures will be the number and type of reported adverse events in subjects and offspring.
- Time frame
- as few as 5 months, up to 16 months
- Population
Source ClinicalTrials.gov
Trial
- Title
- Pregnancy in Polycystic Ovary Syndrome II
- NCT number
- NCT00719186
- Phases
- PHASE3
- Conditions
- Pregnancy, Polycystic Ovary Syndrome
- Interventions
- Clomiphene citrate, Letrozole
- Lead sponsor
- Yale University
- Results first posted
- 2014-06-09
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT00719186?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/NCT00719186-05e3000b