grant

1/3 A randomized controlled trial of frozen embryo transfers performed in modified natural versus programmed cycles (NatPro)

Organization JOHNS HOPKINS UNIVERSITYLocation BALTIMORE, UNITED STATESPosted 26 Sept 2019Deadline 31 Aug 2026
NIHUS FederalResearch GrantFY20230-11 years oldAddressAffectAquadiolAssisted Reproduction TechnologyAssisted Reproductive TechnologyAutologousBirth RateBlindedCardiovascularCardiovascular Body SystemCardiovascular Organ SystemCardiovascular systemCategoriesChildChild YouthChildren (0-21)CirculationClinicalClinical DataCorpus Luteum HormoneCryofixationCryopreservationDataDelta4-pregnene-3,20-dioneDevelopmentDiagnosisDimenformonDiogynDiogynetsEPH GestosisEchographyEchotomographyEmbryoEmbryo TransferEmbryonicEndocrine Gland SecretionEndometrialEndometrial CyclesEnrollmentEnsureEstraceEstradiolEstradiol-17 betaEstradiol-17betaEstraldineFertilization in VitroFetal DeathFetal GrowthFetusFreezingFutureGestationGonadal Steroid HormonesHeart VascularHormonalHormonesHumanHypertensionHypophysisHypophysis CerebriHypothalamic structureHypothalamusIncidenceInfantLiteratureLive BirthMaternal HealthMaternal MortalityMaternal PhysiologyMaternal and Child HealthMedical RecordsMedical UltrasoundMeta-AnalysisMethodsMiscarriageMissionModern ManMothersNICHDNational Institute of Child Health and Human DevelopmentNational Institute of Children's Health and Human DevelopmentNational Institutes of HealthOvocyclinOvocylinOvulationP01 MechanismP01 ProgramParticipantPhysiologicPhysiologicalPituitaryPituitary GlandPituitary Nervous SystemPlayPopulationPre-EclampsiaPre-implantation genetic diagnosisPre-implantation genetic testingPreeclampsiaPregn-4-ene-3,20-dionePregnancyPregnancy ToxemiasPregnenedionePreimplantation DiagnosisPreimplantation Genetic DiagnosisPreimplantation genetic testingPreimplantation testingPreparationProceduresProgesteroneProgram Project GrantProgram Research Project GrantsProgynonProspective, cohort studyProteinuria-Edema-Hypertension GestosisProtocolProtocols documentationRandomization trialRandomizedRandomized, Controlled TrialsRelaxinResearchResearch Program ProjectsResearch ProposalsRiskRoleSafetySex HormonesSex Steroid HormonesSiteSpontaneous abortionStandardizationTest-Tube FertilizationTestingTherapeutic EstradiolTherapeutic HormoneTherapeutic ProgesteroneTreatment ProtocolsTreatment RegimenTreatment ScheduleUltrasonic ImagingUltrasonogramUltrasonographyUltrasound DiagnosisUltrasound Medical ImagingUltrasound TestUnited StatesUnited States National Institutes of HealthVEGFVEGFsVascular Endothelial Growth FactorsVascular Hypertensive DiseaseVascular Hypertensive DisorderWomanadjudicationadjudicative process and procedurearmassisted reproductionassistive reproductive technologycirculatory systemcold preservationcold storagecorpus luteumdesigndesigningdevelopmentaldiagnostic ultrasoundeggembryo cryopreservationembryo freezingembryo transplantationembryonic cryopreservationembryonic freezingenrollfetus deathgonadal steroidshigh blood pressurehyperpiesiahyperpiesishypertensive diseasehypertensive disorderhypothalamicimplantationintra-uterine growthintrauterine growthkidsmaternal deathmaternal outcomemother outcomepre-eclampticpredictive biomarkerspredictive markerpredictive molecular biomarkerpregnancy disorderpregnancy toxemia/hypertensionpreparationsrandomisationrandomizationrandomized control trialrandomized trialrandomized, clinical trialsrandomly assignedresponserisk minimizationsex steroidsocial rolesonogramsonographysound measurementtreatment groupultrasound imagingultrasound scanningyoungster
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Full Description

PROJECT SUMMARY
Of the estimated 1.6 million cycles of assisted reproductive technology (ART) performed globally in one year,

nearly one third are categorized as frozen embryo transfer (FET). In the United States, over half of the ART

cycles involve FET or freezing of all embryos. Given this widespread use of FET, it is of serious concern that

multiple studies have demonstrated an association of FET with an increased risk for hypertensive disorders of

pregnancy, including preeclampsia. It is critical that this risk be minimized because preeclampsia is associated

with severe short- and long-term consequences for both mother and infant, including maternal mortality and fetal

death. Furthermore, several recent meta-analyses emphasized that the evidence to guide clinicians about

protocol choice for optimizing live birth rate with FET is poor.

Our group has recently completed an NIH-sponsored Program Project Grant, with findings that strongly implicate

one commonly performed FET protocol as an explanation for the increased risk of preeclampsia seen with FET.

In a prospective cohort study, one protocol (the programmed FET) was associated with significantly higher rates

of preeclampsia compared with an alternative protocol (the natural cycle FET). Furthermore, through detailed

examination of maternal cardiovascular adaptation to pregnancy in two separate populations, perturbations of

concern were seen with programmed FET, but not with natural cycle FET.

Given these data and other findings in the literature, our central hypothesis is that pregnancy resulting from

an FET in a natural cycle will have a lower rate of preeclampsia compared to an FET in a programmed

cycle. To test this hypothesis, we will conduct a randomized, clinical trial at 6 sites. Our Primary Specific Aim

is to determine the incidence of preeclampsia with the natural versus the programmed cycle. Our second

hypothesis is that the live birth rate following transfer in a natural cycle is similar to that in a programmed FET,

to be tested through a Second Specific Aim in which we compare the live birth rate with the natural versus the

programmed cycle. All embryos will have been created prior to enrollment in the trial and no embryo will be

subjected to increased risk in the course of this research.

With successful completion of this protocol, we will have established the live birth rates for natural cycle FET

compared to a programmed FET cycle, utilizing contemporary standardized protocols. If the natural cycle is

confirmed to be associated with a lower risk of preeclampsia, this study will enhance the safety of ART for millions

of women who are undergoing FET worldwide. This research proposal is highly responsive to the RFA and the

overall mission of NICHD and NIH, as it will not only compare the live birth rates associated with two commonly

used contemporary FET protocols, but it will perhaps even more importantly, compare the safety of these FET

protocols with respect to maternal health.

Grant Number: 5R01HD100341-05
NIH Institute/Center: NIH

Principal Investigator: Valerie Baker

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