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Trial · NCT03703700

Registered outcomes22

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryLive Birth Rate1 year after embryo transfer day, up to a maximum duration of 58 weeksLive birth rate=Number of live birth / Paticipants randomized
SecondaryNumber of Retrieved OocytesOn embryo transfer day, approximately 6 weeksThe total number of oocytes retrieved through ultrasound-guided transvaginal aspiration.
SecondaryRate of Retrieved OocytesOn embryo transfer day, approximately 6 weeksRate of retrieved oocytes =Number of retrieved oocytes/Number of follicles with a diameter ≥10mm on the HCG injection day.
SecondaryNumber of Matured Oocytes RetrievedOn embryo transfer day, approximately 6 weeksThe number of oocytes with pronuclei or polar bodies observed on Day 1 after oocyte retrieval in IVF patients, or as the number of MII oocytes on the day of oocyte retrieval in ICSI patients.
SecondaryRate of Matured OocytesOn embryo transfer day, approximately 6 weeksRate of mature oocytes = Number of mature oocytes/Number of retrieved oocytes
SecondaryNumber of CleavageOn embryo transfer day, approximately 6 weeksNumber of fertilized oocytes that undergo cleavage on Day 2 after oocyte retrieval.
SecondaryCleavage RateOn embryo transfer day, approximately 6 weeksCleavage rate=Number of all cleaved embryos/Number of fertilized oocytes (2PN+1PN+ multiple PN)
SecondaryNumber of Available EmbryosOn embryo transfer day, approximately 6 weeksThe sum of the number of embryos transferred and the number of embryos frozen.
SecondaryRate of Available EmbryosOn embryo transfer day, approximately 6 weeksRate of available embryos=Number of available embryos/Number of cleaved oocytes.
SecondaryNumber of High-quality EmbryosOn embryo transfer day, approximately 6 weeks
High-quality embryo will be defined according to the day of embryo transfer, following the Istanbul consensus and Gardner criteria, Day 2: 4 cells, cell fragments \<10% and no multi-nucleus; Day 3: 8 cells, cell fragments \<10%, no multi-nucleus; Day 5: stage 4 blastocyst, grade A inner cell mass, grade A trophectoderm (12,13).
SecondaryRate of High-quality EmbryosOn embryo transfer day, approximately 6 weeksRate of high-quality embryos=Number of high-quality embryos/Number of available embryos
SecondaryBiochemical Pregnancy Rate14 days after ET day, approximately 8 weeksBiochemical pregnancy rate=Number of positive pregnancy tests/Paticipants randomized
SecondaryImplantation Ratefive weeks after ET day, approximately 11 weeksImplantation rate=Number of gestational sacs/Number of embryos transferred
SecondaryClinical Pregnancy Ratefive weeks after ET day, approximately 11 weeksThe clinical pregnancy determined by the ultrasound, and Clinical pregnancy rate=Number of clinical pregnancies / Paticipants randomized
SecondaryMiscarriage Rate (Among Positive Pregnancy Test Population)1 year after embryo transfer, up to 58 weeksMiscarriage Rate (among positive pregnancy test population) =Number of miscarriages / Number of biochemical pregnancy
SecondaryMiscarriage Rate (Among Clinical Pregnancy Population)1 year after embryo transfer, up to 58 weeksMiscarriage rate (among clinical pregnancy population)=Number of miscarriages / Number of clinical pregnancies
SecondaryThe Birth Weight of the Newborn1 year after embryo transfer, up to 58 weeksBy checking medical records
SecondaryThe Birth Height of the Newborn1 year after embryo transfer, up to 58 weeksBy checking medical records
SecondaryPreterm Delivery Among Live Birth1 year after embryo transfer, up to 58 weeksDelivery of a fetus at less than 37 and more than 28 weeks gestational age.
SecondaryLow Birth Weight Among Neonates1 year after embryo transfer, up to 58 weeksNeonatal birth weight ≤ 2500 g.

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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