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Retrovirus Epidemiology Donor Study-II (REDS-II)

To conduct epidemiological, laboratory, and survey research on volunteer blood donors within the United States to ensure the safety and availability of the United States' blood supply.

Studieoversikt

Detaljert beskrivelse

BACKGROUND:

REDS-I was established to address important blood safety issues involving human retroviruses. On July 17, 1989 the NHLBI awarded contracts to five major blood centers and a coordinating center to develop a major multicenter epidemiologic study of the human retroviruses HIV-1, HIV-2, HTLV-I, and HTLV-II in volunteer U.S. blood donors. The original mission of REDS-I was to initiate and facilitate investigations of human retroviruses in volunteer blood donors from areas of the country at varying risk for HIV. During the course of the project, NHLBI expanded the original REDS-I mission to investigate critical questions posed by the blood banking and transfusion medicine communities that were essential to ensuring an adequate blood supply without compromising blood safety. The overall REDS-I program includes epidemiologic, laboratory, and clinical investigations, and provides a comprehensive framework for monitoring U.S. blood donations, and more recently transfusion recipients, for infectious disease markers. The operational and database structure of REDS-I, specifically designed to study U.S. blood safety and availability, has also provided a framework for rapid analytical response to other research questions of significant importance to the safety of the blood supply. Since its inception, investigators have made major contributions in assessing: the risk of contracting transfusion-transmitted infectious agents; HIV and HCV test screening; donor characteristics and behaviors; and ways of reducing HIV risk from transfusion. REDS-I investigators work closely with the Food and Drug Administration (FDA), Centers for Disease Control and Prevention (CDC) and Office of the Secretary, Department of Health and Human Services (DHHS) to provide data and analyses for important policy decisions. Liaisons with test manufacturers have enabled the rapid study of test procedures of critical importance to blood safety and availability.

DESIGN NARRATIVE:

The objectives of the Retrovirus Epidemiology Donor Study-II (REDS-II) are to conduct epidemiological, laboratory, and survey research on volunteer blood donors within the United States to ensure the safety and availability of the United States' blood supply. This includes monitoring known blood-borne infectious agents, rapidly evaluating the impact of emerging pathogens, assessing the safety implications of changes in laboratory and/or blood donor screening protocols and examining blood supply and availability issues. Addressing issues concerned with the safety and availability of the United States' blood supply will be the cornerstone of the National Heart, Lung, and Blood Institute's Retrovirus Epidemiology Donor Study. These issues include: a) the risks of transfusion-transmissible infections and their trends through time--these include infectious agents currently undergoing laboratory screening as well as new and emerging agents such as West Nile Virus (WNV) which is about to be screened for in the U.S. under experimental protocols; b) ways to reduce the risks of transfusion-transmissible infections; c) HIV, HTLV, HCV, and HBV test screening methodologies; d) donor characteristics, behaviors, and donation return patterns of U.S. blood donors; and e) the effectiveness and safety of various strategies implemented to increase the U.S. blood supply.

Studietype

Observasjonsmessig

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

Ikke eldre enn 100 år (Barn, Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

No eligibility criteria

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

  • Michael Busch, Blood Systems Research Institute
  • Jerome Gottschall, Blood Center of Southeastern Wisconsin, Inc.
  • Christopher Hillyer, Emory University
  • Ram Kakaiya, Institute for Transfusion Medicine
  • Edward Murphy, University of California, San Francisco
  • Jorge Rios, American Red Cross Blood Services, New England Region
  • Ronald Sacher, University of Cincinnati
  • George Schreiber, Westat, Inc.

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart

1. september 2004

Primær fullføring (Faktiske)

1. september 2009

Studiet fullført (Faktiske)

1. september 2009

Datoer for studieregistrering

Først innsendt

17. november 2004

Først innsendt som oppfylte QC-kriteriene

17. november 2004

Først lagt ut (Anslag)

18. november 2004

Oppdateringer av studieposter

Sist oppdatering lagt ut (Anslag)

15. april 2016

Siste oppdatering sendt inn som oppfylte QC-kriteriene

14. april 2016

Sist bekreftet

1. september 2009

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

Studiedata/dokumenter

  1. Datasett for individuell deltaker
    Informasjonsidentifikator: REDS II-CORE
    Informasjonskommentarer: NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
  2. Håndbok for prosedyrer
    Informasjonsidentifikator: REDS II-CORE
  3. Datasett for individuell deltaker
    Informasjonsidentifikator: REDS II-LAPS
    Informasjonskommentarer: NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
  4. Studieprotokoll
    Informasjonsidentifikator: REDS II-LAPS
  5. Studieskjemaer
    Informasjonsidentifikator: REDS II-LAPS
  6. Håndbok for prosedyrer
    Informasjonsidentifikator: REDS II-LAPS
  7. Datasett for individuell deltaker
    Informasjonsidentifikator: REDS II-MS
    Informasjonskommentarer: NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
  8. Studieprotokoll
    Informasjonsidentifikator: REDS II-MS
  9. Håndbok for prosedyrer
    Informasjonsidentifikator: REDS II-MS
  10. Datasett for individuell deltaker
    Informasjonsidentifikator: REDS II-RISE
    Informasjonskommentarer: NHLBI provides controlled access to IPD through BioLINCC. Access requires registration, evidence of local IRB approval or certification of exemption from IRB review, and completion of a data use agreement.
  11. Studieprotokoll
    Informasjonsidentifikator: REDS II-RISE
  12. Studieskjemaer
    Informasjonsidentifikator: REDS II-RISE
  13. Håndbok for prosedyrer
    Informasjonsidentifikator: REDS II-RISE

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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