- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT00097006
Retrovirus Epidemiology Donor Study-II (REDS-II)
Aperçu de l'étude
Statut
Description détaillée
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.
Type d'étude
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
La description
Plan d'étude
Comment l'étude est-elle conçue ?
Collaborateurs et enquêteurs
Les enquêteurs
- 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.
Publications et liens utiles
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude
Achèvement primaire (Réel)
Achèvement de l'étude (Réel)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Estimation)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Estimation)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
- Maladies du système digestif
- Processus pathologiques
- Infections par virus à ARN
- Maladies virales
- Infections transmissibles par le sang
- Maladies sexuellement transmissibles, virales
- Maladies sexuellement transmissibles
- Infections à lentivirus
- Maladies du système immunitaire
- Attributs de la maladie
- Maladies du foie
- Infections à Hépadnaviridae
- Infections par le virus de l'ADN
- Infections à entérovirus
- Infections à Picornaviridae
- Maladies à virus lents
- Infections à VIH
- Infections
- Maladies transmissibles
- Hépatite B
- Hépatite
- Hépatite A
- Syndrome immunodéficitaire acquis
- Syndromes d'immunodéficience
- Hépatite, virale, humaine
- Infections à rétroviridae
Autres numéros d'identification d'étude
- 1243
Plan pour les données individuelles des participants (IPD)
Données/documents d'étude
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Ensemble de données de participant individuel
Identifiant des informations: REDS II-CORECommentaires d'informations: 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.
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Manuel de Procédures
Identifiant des informations: REDS II-CORE
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Ensemble de données de participant individuel
Identifiant des informations: REDS II-LAPSCommentaires d'informations: 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.
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Protocole d'étude
Identifiant des informations: REDS II-LAPS
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Formulaires d'étude
Identifiant des informations: REDS II-LAPS
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Manuel de Procédures
Identifiant des informations: REDS II-LAPS
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Ensemble de données de participant individuel
Identifiant des informations: REDS II-MSCommentaires d'informations: 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.
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Protocole d'étude
Identifiant des informations: REDS II-MS
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Manuel de Procédures
Identifiant des informations: REDS II-MS
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Ensemble de données de participant individuel
Identifiant des informations: REDS II-RISECommentaires d'informations: 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.
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Protocole d'étude
Identifiant des informations: REDS II-RISE
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Formulaires d'étude
Identifiant des informations: REDS II-RISE
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Manuel de Procédures
Identifiant des informations: REDS II-RISE
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