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Comparison · NCT01075815-2182888e

rFSH + rhLH vs rFSH: Number of Participants With Biochemical Pregnancies

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. rFSH + rhLH vs rFSH: Number of Participants With Biochemical Pregnancies. Trial comparisons, record NCT01075815-2182888e. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01075815-2182888e

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.2750.1610.428wilson
Risk in group 20.2860.1630.451wilson
Risk difference, group 1 minus group 2-0.0107-0.2110.186newcombe hybrid score
Risk ratio, group 1 over group 20.9630.4661.99log
Odds ratio, group 1 over group 20.9480.3452.6log
Number needed to treat, for one fewer participant with the outcome on rFSH + rhLH than on rFSH93.3from the risk difference intervalthe interval includes no difference

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1rFSH + rhLH
Recombinant human luteinizing hormone (rhLH, Luveris®) injection 150 International Units (IU) subcutaneously daily along with recombinant follicle-stimulating hormone (rFSH) 300 IU subcutaneously daily from Day 1 of stimulation period (S1) to Day 4 of stimulation period (S4) and then rFSH dose adjusted depending on the ovarian response till recombinant human choriogonadotropin (r-hCG) administration day.
1140OG000
Group 2rFSHRecombinant follicle stimulating hormone (rFSH) injection 300 IU subcutaneously daily from S1 to S4 and then dose adjusted depending on the ovarian response till r-hCG administration day.1035OG001

Outcome

Type
SECONDARY
Title
Number of Participants With Biochemical Pregnancies
Description
Biochemical pregnancy was defined as a pregnancy diagnosed only by the detection of hCG in serum or urine and that does not develop into a clinical pregnancy.
Time frame
2 months after OPU (34-38 hours post r-hCG day {end of stimulation cycle} [approximately 28 days])
Population
ITT population included all randomized participants who had received at least 1 dose of the study medication.

Source ClinicalTrials.gov

Trial

Title
A Clinical Trial to Determine the Effect of Lutropin Alfa on Embryo Quality and Implantation Rate in Advanced Reproductive Age
NCT number
NCT01075815
Phases
PHASE2
Conditions
Infertility, Ovulation Induction
Interventions
Recombinant human luteinizing hormone (rhLH), Recombinant follicle-stimulating hormone (rFSH)
Lead sponsor
Merck KGaA, Darmstadt, Germany
Results first posted
2012-11-20

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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