Status
Active
Acronym
EuroSIDA
NCT (clinicaltrials.gov)
NCT02699736

EUROSIDA Kohorte

Purpose / Objectives

Primary Outcome

EuroSIDA’s primary objective is to prospectively study clinical, therapeutic, demographic, virological and laboratory data as well as plasma from people living with HIV across Europe to determine the long-term virological, immunological and clinical outcome in a large cohort of consecutive enrolled study participants. The specific objectives, falling into four main categories, are as follows:   

  • To assess the factors associated with the clinical, immunological and virological course of HIV infection and HIV-related co-infections and co-morbidities  
  • To detect current or emerging late onset adverse events among persons on ART 
  • To continue surveillance of HIV in clinics around Europe to describe temporal changes and regional difference
  • To investigate the long-term clinical outcomes of common co-infections and co-morbidities and the impact of treatment

Secondary Outcomes

na

Diagnosis

  • HIV-1
  • Infectiology/HIV and AIDS

HIV

Target population

Disease stage

HIV

Age

18-99

Inclusion criteria

HIV-1 Infection

Exclusion criteria

na

Study design

  • Multicenter
  • Retrospective
  • Tumor Biology, Infection and Immunity
  • Cohort

Intervention

na

Documents (password protected)

Responsibilities in overall study

Sponsor

CHIP Kopenhagen

  • Tel. +45 35 45 5757
  • Fax +45 35 45 5758