Comparison · NCT03846544-c01b3a39
Double Pick up Group vs Control Group: Clinical Pregnancy Rates
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. Double Pick up Group vs Control Group: Clinical Pregnancy Rates. Trial comparisons, record NCT03846544-c01b3a39. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03846544-c01b3a39
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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 | 0.565 | 0.368 | 0.744 | wilson | |
| Risk in group 2 | 0.304 | 0.156 | 0.509 | wilson | |
| Risk difference, group 1 minus group 2 | 0.261 | -0.023 | 0.493 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 1.86 | 0.909 | 3.79 | log | |
| Odds ratio, group 1 over group 2 | 2.97 | 0.884 | 9.98 | log | |
| Number needed to treat, for one more participant with the outcome on Double Pick up Group than on Control Group | 3.83 | from the risk difference interval | the interval includes no difference |
Source ClinicalTrials.gov
Groups2
Group 2 names the comparator: control.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | Double Pick up Group | CFA-double pick up: In the study group, 225 IU of rFSH will continue after the first oocyte retrieval (OR). Antagonist administration will be initiated when at least one follicle measuring ≥14 mm will be present in the ultrasound. If one or more follicles ≥17 mm are observed, patients will undergo a second triggering with hCG 5000 IU and a second OR will be performed. In case of patients with no follicular development following 10 additional days of rFSH post-OR | 13 | 23 | OG001 |
| Group 2 | Control Group | conventional stimulation group | 7 | 23 | OG000 |
Source ClinicalTrials.gov
Outcome
- Type
- SECONDARY
- Title
- Clinical Pregnancy Rates
- Description
- clinical pregnancy rate
- Time frame
- 4 months
- Population
Source ClinicalTrials.gov
Trial
- Title
- Double Pick up in Poor Prognosis Women
- NCT number
- NCT03846544
- Phases
- PHASE4
- Conditions
- Fertility Disorders
- Interventions
- Corifollitoropin alfa (CFA)-double pick up
- Lead sponsor
- CRG UZ Brussel
- Results first posted
- 2024-04-15
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT03846544?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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