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Trial · NCT03296527

Results by group242

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Ongoing Pregnancy RateFE 000049 (Follitropin Delta)31.3percentage of participants
Ongoing Pregnancy RateGONAL-F (Follitropin Alfa)25.7percentage of participants
Positive Beta Unit of Human Chorionic Gonadotropin (βhCG) RateFE 000049 (Follitropin Delta)41.7percentage of participants
Positive Beta Unit of Human Chorionic Gonadotropin (βhCG) RateGONAL-F (Follitropin Alfa)35.3percentage of participants
Clinical Pregnancy RateFE 000049 (Follitropin Delta)36.1percentage of participants
Clinical Pregnancy RateGONAL-F (Follitropin Alfa)31.2percentage of participants
Vital Pregnancy RateFE 000049 (Follitropin Delta)32.3percentage of participants
Vital Pregnancy RateGONAL-F (Follitropin Alfa)28.0percentage of participants
Implantation RateFE 000049 (Follitropin Delta)35.6percentage of sacs/embryos transferred
Implantation RateGONAL-F (Follitropin Alfa)31.3percentage of sacs/embryos transferred
Ongoing Implantation RateFE 000049 (Follitropin Delta)30.7% of viable fetus/embryos transferred
Ongoing Implantation RateGONAL-F (Follitropin Alfa)25.8% of viable fetus/embryos transferred
Proportion of Subjects With Extreme Ovarian ResponsesFE 000049 (Follitropin Delta)<4 or >=15 oocytes retrieved30.3percentage of participants
Proportion of Subjects With Extreme Ovarian ResponsesGONAL-F (Follitropin Alfa)<4 or >=15 oocytes retrieved35.1percentage of participants
Proportion of Subjects With Extreme Ovarian ResponsesFE 000049 (Follitropin Delta)<4 or >=20 oocytes retrieved17.4percentage of participants
Proportion of Subjects With Extreme Ovarian ResponsesGONAL-F (Follitropin Alfa)<4 or >=20 oocytes retrieved18.9percentage of participants
Proportion of Subjects With Early OHSS (Including OHSS of Moderate/Severe Grade) and/or Preventive Interventions for Early OHSSFE 000049 (Follitropin Delta)Early OHSS (any grade)4.0percentage of participants
Proportion of Subjects With Early OHSS (Including OHSS of Moderate/Severe Grade) and/or Preventive Interventions for Early OHSSGONAL-F (Follitropin Alfa)Early OHSS (any grade)6.5percentage of participants
Proportion of Subjects With Early OHSS (Including OHSS of Moderate/Severe Grade) and/or Preventive Interventions for Early OHSSFE 000049 (Follitropin Delta)Early OHSS (moderate/severe)3.6percentage of participants
Proportion of Subjects With Early OHSS (Including OHSS of Moderate/Severe Grade) and/or Preventive Interventions for Early OHSSGONAL-F (Follitropin Alfa)Early OHSS (moderate/severe)4.7percentage of participants

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
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
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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