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Trial · NCT03228680

Results by group156

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

OutcomeGroupCategoryValueSpreadUnits
Proportion of Participants With <4, 4-7, 8-14, 15-19 and ≥20 Oocytes RetrievedFE 999049 (Follitropin Delta)Targeted response (8-14 oocytes)40.8percentage of participants
Proportion of Participants With <4, 4-7, 8-14, 15-19 and ≥20 Oocytes RetrievedFOLLISTIM (Follitropin Beta)Targeted response (8-14 oocytes)42.8percentage of participants
Proportion of Participants With <4, 4-7, 8-14, 15-19 and ≥20 Oocytes RetrievedFE 999049 (Follitropin Delta)Hyperresponse (15-19 oocytes)10.1percentage of participants
Proportion of Participants With <4, 4-7, 8-14, 15-19 and ≥20 Oocytes RetrievedFOLLISTIM (Follitropin Beta)Hyperresponse (15-19 oocytes)14.5percentage of participants
Proportion of Participants With <4, 4-7, 8-14, 15-19 and ≥20 Oocytes RetrievedFE 999049 (Follitropin Delta)Severe hyperresponse (≥ 20 oocytes)4.7percentage of participants
Proportion of Participants With <4, 4-7, 8-14, 15-19 and ≥20 Oocytes RetrievedFOLLISTIM (Follitropin Beta)Severe hyperresponse (≥ 20 oocytes)11.0percentage of participants
Proportion of Participants With Extreme Ovarian Responses (Defined as <4, ≥15 or ≥20 Oocytes Retrieved) in Risk PopulationFE 999049 (Follitropin Delta)AMH < 15 pmol/L (<4 oocytes retrieved)11.6percentage of participants
Proportion of Participants With Extreme Ovarian Responses (Defined as <4, ≥15 or ≥20 Oocytes Retrieved) in Risk PopulationFOLLISTIM (Follitropin Beta)AMH < 15 pmol/L (<4 oocytes retrieved)12.3percentage of participants
Proportion of Participants With Extreme Ovarian Responses (Defined as <4, ≥15 or ≥20 Oocytes Retrieved) in Risk PopulationFE 999049 (Follitropin Delta)AMH >= 15 pmol/L (>=15 oocytes retrieved)22.0percentage of participants
Proportion of Participants With Extreme Ovarian Responses (Defined as <4, ≥15 or ≥20 Oocytes Retrieved) in Risk PopulationFOLLISTIM (Follitropin Beta)AMH >= 15 pmol/L (>=15 oocytes retrieved)42.0percentage of participants
Proportion of Participants With Extreme Ovarian Responses (Defined as <4, ≥15 or ≥20 Oocytes Retrieved) in Risk PopulationFE 999049 (Follitropin Delta)AMH >= 15 pmol/L (>=20 oocytes retrieved)8.0percentage of participants
Proportion of Participants With Extreme Ovarian Responses (Defined as <4, ≥15 or ≥20 Oocytes Retrieved) in Risk PopulationFOLLISTIM (Follitropin Beta)AMH >= 15 pmol/L (>=20 oocytes retrieved)19.0percentage of participants
Proportion of Participants With Preventive Interventions for Early Ovarian Hyperstimulation Syndrome (OHSS)FE 999049 (Follitropin Delta)Cycle cancellation0percentage of participants
Proportion of Participants With Preventive Interventions for Early Ovarian Hyperstimulation Syndrome (OHSS)FOLLISTIM (Follitropin Beta)Cycle cancellation1.1percentage of participants
Proportion of Participants With Preventive Interventions for Early Ovarian Hyperstimulation Syndrome (OHSS)FE 999049 (Follitropin Delta)Triggering with GnRH agonist1.2percentage of participants
Proportion of Participants With Preventive Interventions for Early Ovarian Hyperstimulation Syndrome (OHSS)FOLLISTIM (Follitropin Beta)Triggering with GnRH agonist1.1percentage of participants
Proportion of Participants With Preventive Interventions for Early Ovarian Hyperstimulation Syndrome (OHSS)FE 999049 (Follitropin Delta)Administration of dopamine agonist0.6percentage of participants
Proportion of Participants With Preventive Interventions for Early Ovarian Hyperstimulation Syndrome (OHSS)FOLLISTIM (Follitropin Beta)Administration of dopamine agonist1.7percentage of participants
Proportions of Participants With Early OHSS (Including OHSS of Moderate/Severe Grade) and/or Preventive Interventions for Early OHSSFE 999049 (Follitropin Delta)Early OHSS (any grade)10.0percentage of participants
Proportions of Participants With Early OHSS (Including OHSS of Moderate/Severe Grade) and/or Preventive Interventions for Early OHSSFOLLISTIM (Follitropin Beta)Early OHSS (any grade)18.6percentage 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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