The RESPOND Outcomes Study

Last updated: April 10, 2024
Sponsor: Rigshospitalet, Denmark
Overall Status: Active - Recruiting

Phase

N/A

Condition

Hiv

Treatment

N/A

Clinical Study ID

NCT04090151
The RESPOND Outcomes Study
  • Ages > 18
  • All Genders

Study Summary

The RESPOND Outcomes study is a research study around use of antiretroviral and other relevant drugs and long-term clinical outcomes in patients living with HIV. Data collected in this study will be used to answer key unanswered questions regarding treatment of people living with HIV.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Signed Informed consent for the Outcomes study, if required by local/nationallegislation
  2. Signed informed consent for the RESPOND consortium and data repository, if required bylocal/national legislation
  3. Age ≥ 18 years of age
  4. Confirmed HIV-1 infection
  5. Persons receiving integrase inhibitor (INSTI) based antiretroviral therapy if havestarted after the later of 1/1/2012 and local cohort enrolment (i.e., duringprospective follow-up in the cohort and after 1/1/2012) and have a CD4 and HIV viralload in the 12 months prior to starting INSTI or within 3 months after starting INSTI.
  6. ART experienced and ART naïve persons not receiving INSTI if have a CD4 and HIV viralload in the 12 months prior to baseline or within 3 months after baseline (here, thelatest of 1/1/2012 or cohort enrolment).
  7. Persons lost to follow-up or who died before RESPOND enrolment should therefore stillbe included in the Outcomes study, provided they satisfy the other inclusion criteria.

Exclusion

Exclusion Criteria:

  1. Persons receiving INSTI before 1/1/2012 are excluded from the Outcome study
  2. Persons aged < 18 at baseline are excluded from the Outcome study

Study Design

Total Participants: 37853
Study Start date:
January 01, 2017
Estimated Completion Date:
December 31, 2025

Study Description

The specific objectives, falling into three main categories, are as follows:

  1. Monitor the uptake of newer antiretroviral treatment (ART) drugs and drugs for treatment of co-infections and co-morbidities;

  2. To evaluate the safety profiles of the newer individual ART drugs when used in routine clinical practice as part of either first-line or subsequent treatment regimens.

  3. Investigate long term outcomes and clinical disease progression overall and in specific sub-groups

The Outcomes study is a collaboration between investigators from clinics and cohorts across Europe, Australia and South America with a willingness to share data and to use a common follow-up schedule and assessment. Participating sites have a commitment to continue to follow this large cohort that is heterogeneous in both its demographic profile and in ART prescribing patterns thus resulting in enough power to answer many key clinical questions.

The Outcomes study is a study in the RESPOND International Cohort Consortium of Infectious Diseases. RESPOND is an innovative, flexible and dynamic cohort consortium for the study of infectious diseases, including HIV, built as a generic structure for facilitating multi stakeholder involvement. In RESPOND all collected data is part of a common data repository or 'data lake', which is stored in a database located at CHIP, Rigshospitalet, Copenhagen, Denmark. Data collection in RESPOND is modular with a core data collection module onto which additional modules/studies can be added. Pseudonymised patient data can be entered manually via an online secure platform or be electronically transferred from existing local, regional or national data structures to the data lake.

In the Outcomes study data will be collected at enrolment and at annual follow-up (FU) visits. For patients living with HIV-1 enrolled and under FU, demographic, laboratory, therapeutic and clinical data on HIV and viral hepatitis will be collected once a year. Clinical event data (except AIDS other than AIDS defining malignancies) will be collected in real-time on RESPOND event forms.

Connect with a study center

  • The Australian HIV Observational Database (AHOD)

    Sydney, New South Wales 2052
    Australia

    Active - Recruiting

  • Austrian HIV Cohort Study (AHIVCOS), Medizinische Universität Innsbruch

    Innsbruck, 6020
    Austria

    Active - Recruiting

  • CHU Saint-Pierre Hospital

    Brussels, 1000
    Belgium

    Active - Recruiting

  • Rigshospitalet

    Copenhagen, 2100
    Denmark

    Active - Recruiting

  • The EuroSIDA Study, CHIP, Rigshospitalet

    Copenhagen, 2100
    Denmark

    Active - Recruiting

  • Nice HIV Cohort, Centre Hospitalier Universitaire de Nice

    Nice,
    France

    Active - Recruiting

  • Georgian National AIDS Health Information System (AIDS HIS), IDACIRC

    Tbilisi,
    Georgia

    Active - Recruiting

  • University Hospital Bonn

    Bonn, 53105
    Germany

    Active - Recruiting

  • University Hospital Cologne

    Cologne, 5093
    Germany

    Active - Recruiting

  • Frankfurt HIV Cohort Study, Goethe-University Frankfurt

    Frankfurt, 60323
    Germany

    Active - Recruiting

  • San Raffaele Scientific Institute, Ospedale San Raffaele

    Milan,
    Italy

    Active - Recruiting

  • Italian Cohort Naive Antiretrovirals (ICONA)

    Milano, 20124
    Italy

    Active - Recruiting

  • Modena HIV Cohort, Università degli Studi di Modena

    Modena, 44100
    Italy

    Active - Recruiting

  • The ATHENA (AIDS Therapy Evaluation in the Netherlands) national observational HIV cohort, Stichting HIV Monitorin, AMC, University of Amsterdam

    Amsterdam, 1105
    Netherlands

    Active - Recruiting

  • PISCIS Cohort Study, Germans Trias i Pujol University Hospital

    Badalona, 08916
    Spain

    Active - Recruiting

  • Swedish InfCare HIV Cohort, Karolinska University Hospital

    Stockholm, 171 76
    Sweden

    Active - Recruiting

  • Swiss HIV Cohort Study (SHCS), University Hospital Zurich

    Zurich, 8091
    Switzerland

    Active - Recruiting

  • Royal Free HIV Cohort Study, Royal Free Hospital

    London, NW3 2 PF
    United Kingdom

    Active - Recruiting

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