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Trial · NCT03738618

Outcomes69

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYCumulative Ongoing Pregnancy Rate After the Fresh Cycle and Cryopreserved Cycles Initiated Within 12 Months From the Start of Controlled Ovarian Stimulation (COS)8-9 weeks after transfer (up to approximately 16 months after start of stimulation)The mITT analysis set comprised all randomized and exposed participants. Participants were analyzed according to planned treatment.percentage of participantsNUMBER
SECONDARYOngoing Pregnancy Rate in the Fresh Cycle and in the Cryopreserved Cycles8-9 weeks after transfer (up to approximately 16 months after start of stimulation)The mITT analysis set comprised all randomized and exposed participants. Participants were analyzed according to planned treatment.percentage of participantsNUMBER
SECONDARYTime From Start of COS to Ongoing Pregnancy Across the Fresh and Cryopreserved Cycles, Including Duration8-9 weeks after transfer (up to approximately 16 months after start of stimulation)The mITT analysis set comprised all randomized and exposed participants. Participants were analyzed according to planned treatment.daysMEAN
SECONDARYTime From Start of COS to Ongoing Pregnancy Across the Fresh and Cryopreserved Cycles, Measured in Number of Cycles Before Achieving Ongoing Pregnancy8-9 weeks after transfer (up to approximately 16 months after start of stimulation)The mITT analysis set comprised all randomized and exposed participants. Participants were analyzed according to planned treatment.CyclesMEAN
SECONDARYOngoing Implantation Rate in the Fresh Cycle, the Cryopreserved Cycles and Cumulatively8-9 weeks after transfer (up to approximately 16 months after start of stimulation)The mITT analysis set comprised all randomized and exposed participants. Participants were analyzed according to planned treatment.% of viable fetus/blastocyst transferNUMBER
SECONDARYClinical Pregnancy Rate in the Fresh Cycle, the Cryopreserved Cycles and Cumulatively5-6 weeks after transfer (up to approximately 15 months after start of stimulation)The mITT analysis set comprised all randomized and exposed participants. Participants were analyzed according to planned treatment.percentage of participantsNUMBER
SECONDARYVital Pregnancy Rate in the Fresh Cycle, the Cryopreserved Cycles and Cumulatively5-6 weeks after transfer (up to approximately 15 months after start of stimulation)The mITT analysis set comprised all randomized and exposed participants. Participants were analyzed according to planned treatment.percentage of participantsNUMBER
SECONDARYImplantation Rate in the Fresh Cycle, the Cryopreserved Cycles and Cumulatively5-6 weeks after transfer (up to approximately 15 months after start of stimulation)The mITT analysis set comprised all randomized and exposed participants. Participants were analyzed according to planned treatment.% gestational sacs/blastocyst transferNUMBER
SECONDARYPositive Beta Human Chorionic Gonadotropin (βhCG) Rate in the Fresh Cycle, the Cryopreserved Cycles and Cumulatively10-14 days after transfer (up to approximately 14 months after start of stimulation)The mITT analysis set comprised all randomized and exposed participants. Participants were analyzed according to planned treatment.percentage of participantsNUMBER
SECONDARYProportion of Subjects in the Fresh Cycle With Triggering of Final Follicular Maturation (With hCG, With GnRH Agonist, and in Total), Cycle Cancellation and Transfer CancellationUp to 5 days after oocyte retrieval (up to 27 days after start of stimulation)The mITT analysis set comprised all randomized and exposed participants. Participants were analyzed according to planned treatment.percentage of participantsNUMBER
SECONDARYNumber of Follicles on Stimulation Day 5On stimulation day 5The mITT analysis set comprised all randomized and exposed participants. Participants were analyzed according to planned treatment.number of folliclesMEAN
SECONDARYNumber of Follicles at End-of-stimulationAt end-of-stimulation (up to 20 stimulation days)The mITT analysis set comprised all randomized and exposed participants. Participants were analyzed according to planned treatment.number of folliclesMEAN
SECONDARYSize of Follicles on Stimulation Day 5On stimulation day 5The mITT analysis set comprised all randomized and exposed participants. Participants were analyzed according to planned treatment.mmMEAN
SECONDARYSize of Follicles at End-of-stimulationAt end-of-stimulation (up to 20 stimulation days)The mITT analysis set comprised all randomized and exposed participants. Participants were analyzed according to planned treatment.mmMEAN
SECONDARYNumber of Oocytes RetrievedOn day of oocyte retrieval (up to 22 days after start of stimulation)The mITT analysis set comprised all randomized and exposed participants. Participants were analyzed according to planned treatment.number of oocytes retrievedMEAN
SECONDARYProportion of Subjects With <4, 4-7, 8-14, 15-19 and ≥20 Oocytes RetrievedOn day of oocyte retrieval (up to 22 days after start of stimulation)The mITT analysis set comprised all randomized and exposed participants. Participants were analyzed according to planned treatment.percentage of participantsNUMBER
SECONDARYNumber of Metaphase II OocytesOn day of oocyte retrieval (up to 22 days after start of stimulation)The mITT analysis set comprised all randomized and exposed participants. Participants were analyzed according to planned treatment.number of MII oocytesMEAN
SECONDARYNumber of Fertilized OocytesOn day 1 after oocyte retrieval (up to 23 days after start of stimulation)The mITT analysis set comprised all randomized and exposed participants. Participants were analyzed according to planned treatment.oocytes (number of fertilized oocytes)MEAN
SECONDARYFertilization RateOn day 1 after oocyte retrieval (up to 23 days after start of stimulation)The mITT analysis set comprised all randomized and exposed participants. Participants were analyzed according to planned treatment.percentage of fertilized oocytesMEAN
SECONDARYNumber and Quality of Blastocysts on Day 5 After Oocyte RetrievalOn day 5 after oocyte retrievalThe mITT analysis set comprised all randomized and exposed participants. Participants were analyzed according to planned treatment.blastocystsMEAN

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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