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Pediatric Heart network DCC

Pediatric Heart network DCC
儿科心脏网络 DCC
批准号:
8681492
负责人:
Julie Elaine Miller
金额:
$895.51万
依托单位国家:
美国
项目类别:
财政年份:
2001
资助国家:
美国
项目状态:
已结题
起止时间:
2001-09-06 至 2015-12-31
关键词:
AddressAdherenceAdolescent and Young AdultAdrenergic beta-AntagonistsAdverse eventAgeArrhythmiaAspirinAtenololBioinformaticsBooksBudgetsCardiologyCardiomyopathiesCardiovascular systemCaringCase Report FormCertificationCessation of lifeChildChildhoodClinicalClinical DataClinical ManagementClinical ResearchClinical TreatmentClinical TrialsCodeCohort StudiesCollaborationsCommon VentricleCommunicationCongenital Heart DefectsContractsCore FacilityCoronary arteryDataData Coordinating CenterData QualityData SetDatabasesDevelopmentDevicesDiagnosticDictionaryDimensionsDiseaseDocumentationEFRACElectronicsEnalaprilEnrollmentEventEvidence Based MedicineExerciseFosteringFundingGeneticGoalsGrowthHealthHealth StatusHeartHeart DiseasesImageInfantInflammatoryInformation SystemsInstitutionIntravenous ImmunoglobulinsJournalsLaboratoriesLeadLeadershipLosartanMagnetic Resonance ImagingMaintenanceManualsManuscriptsMarfan SyndromeMeasurementMeasuresMedicalMedical centerMethylprednisoloneMissionMonitorMulti-Institutional Clinical TrialMyocardiumMyopathyNational Heart, Lung, and Blood InstituteNew EnglandObservational StudyOccupational activity of managing financesOnline SystemsOperative Surgical ProceduresOutcomeParentsPerformancePersonsPharmaceutical PreparationsPhysiologic pulsePlacebosPlant RootsPlayPoliciesPositioning AttributePreparationPrincipal InvestigatorProceduresProcessProductionProgram DevelopmentProtocols documentationPublicationsPublishingPulmonary artery structureQuality ControlQuality of lifeRandomizedReadingRegistriesReportingResearchResearch DesignResearch InfrastructureResearch InstituteResearch PersonnelResearch SupportResourcesRoleSafetySample SizeScheduleScienceScientistSecureSerologic testsServicesShunt DeviceSiteSteroidsSystemTeleconferencesTestingTimeTrainingTranslational ResearchTransplantationVentricularVisitWeightWorkWritingbiobankclinical research sitecongenital heart disordercostdata acquisitiondata exchangedata sharingdesigndistributed dataexperiencefollow-uphigh standardimprovedinnovationmeetingsnoveloperationpaymentprogramsprotocol developmentquality assuranceracial and ethnic disparitiesrandomized trialreconstructionrepositoryresearch studystatisticssymposiumtoolweb site

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DESCRIPTION (provided by applicant): New England Research Institutes, Inc. (NERI) is applying to continue its 10-year role as the Data Coordinating Center (DCC) for the Pediatric Heart Network (PHN). The PHN will continue as a cooperative network of up to 8 Clinical Centers, 15 auxiliary sites, a DCC, a Network Chair, and NHLBI Project Scientists. The objectives of the PHN are to 1) provide an infrastructure for multi-center collaborative clinical research, and 2) to evaluate diagnostic, medical, interventional, and surgical therapies for congenital heart defects, inflammatory heart disease, heart muscle disease, and arrhythmias. As the DCC, NERI will continue to provide scientific and logistical support for the next cycle of the Network, with key responsibilities and functions for leadership in study design and statistics, overall study coordination and management of data acquisition; leadership in development activities for bioinformatics infrastructure and tools; electronic information and data systems; logistical and support services; and management and distribution of Network funds. A multiple PI leadership plan is proposed to continue the leadership roles shared by Dr. Sleeper (Clinical and Statistical Science) and Dr. Tennstedt (Network Operations), with clearly delineated roles and responsibilities for leading and directing the DCC, intellectually and operationally. Importantly, the DCC staff will be organized to include a Network Manager who is also the Manager for the NHLBI Bench to Bassinet Program. This will position the DCC to facilitate integration of the PHN as the clinical trials component of the B2B Program. RELEVANCE: The mission of the Pediatric Heart Network is to improve the health and quality of life for children, adolescents, and young adults who are born with heart defects or develop heart disease by conducting large clinical studies at many medical centers. The Data Coordinating Center provides important services to guide and support this research.
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