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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.

Studieöversikt

Detaljerad beskrivning

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.

Studietyp

Observationell

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

Inte äldre än 100 år (Barn, Vuxen, Äldre vuxen)

Tar emot friska volontärer

Nej

Kön som är behöriga för studier

Allt

Beskrivning

No eligibility criteria

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Utredare

  • 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.

Publikationer och användbara länkar

Den som ansvarar för att lägga in information om studien tillhandahåller frivilligt dessa publikationer. Dessa kan handla om allt som har med studien att göra.

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart

1 september 2004

Primärt slutförande (Faktisk)

1 september 2009

Avslutad studie (Faktisk)

1 september 2009

Studieregistreringsdatum

Först inskickad

17 november 2004

Först inskickad som uppfyllde QC-kriterierna

17 november 2004

Första postat (Uppskatta)

18 november 2004

Uppdateringar av studier

Senaste uppdatering publicerad (Uppskatta)

15 april 2016

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

14 april 2016

Senast verifierad

1 september 2009

Mer information

Termer relaterade till denna studie

Plan för individuella deltagardata (IPD)

Studiedata/dokument

  1. Datauppsättning för individuella deltagare
    Informationsidentifierare: REDS II-CORE
    Informationskommentarer: 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. Handbok för procedurer
    Informationsidentifierare: REDS II-CORE
  3. Datauppsättning för individuella deltagare
    Informationsidentifierare: REDS II-LAPS
    Informationskommentarer: 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
    Informationsidentifierare: REDS II-LAPS
  5. Studieformulär
    Informationsidentifierare: REDS II-LAPS
  6. Handbok för procedurer
    Informationsidentifierare: REDS II-LAPS
  7. Datauppsättning för individuella deltagare
    Informationsidentifierare: REDS II-MS
    Informationskommentarer: 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
    Informationsidentifierare: REDS II-MS
  9. Handbok för procedurer
    Informationsidentifierare: REDS II-MS
  10. Datauppsättning för individuella deltagare
    Informationsidentifierare: REDS II-RISE
    Informationskommentarer: 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
    Informationsidentifierare: REDS II-RISE
  12. Studieformulär
    Informationsidentifierare: REDS II-RISE
  13. Handbok för procedurer
    Informationsidentifierare: REDS II-RISE

Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .

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