Phase
Condition
Hiv
Treatment
N/AClinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Signed Informed consent for the Outcomes study, if required by local/nationallegislation
- Signed informed consent for the RESPOND consortium and data repository, if required bylocal/national legislation
- Age ≥ 18 years of age
- Confirmed HIV-1 infection
- 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.
- 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).
- 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:
- Persons receiving INSTI before 1/1/2012 are excluded from the Outcome study
- Persons aged < 18 at baseline are excluded from the Outcome study
Study Design
Study Description
Connect with a study center
The Australian HIV Observational Database (AHOD)
Sydney, New South Wales 2052
AustraliaActive - Recruiting
Austrian HIV Cohort Study (AHIVCOS), Medizinische Universität Innsbruch
Innsbruck, 6020
AustriaActive - Recruiting
CHU Saint-Pierre Hospital
Brussels, 1000
BelgiumActive - Recruiting
Rigshospitalet
Copenhagen, 2100
DenmarkActive - Recruiting
The EuroSIDA Study, CHIP, Rigshospitalet
Copenhagen, 2100
DenmarkActive - Recruiting
Nice HIV Cohort, Centre Hospitalier Universitaire de Nice
Nice,
FranceActive - Recruiting
Georgian National AIDS Health Information System (AIDS HIS), IDACIRC
Tbilisi,
GeorgiaActive - Recruiting
University Hospital Bonn
Bonn, 53105
GermanyActive - Recruiting
University Hospital Cologne
Cologne, 5093
GermanyActive - Recruiting
Frankfurt HIV Cohort Study, Goethe-University Frankfurt
Frankfurt, 60323
GermanyActive - Recruiting
San Raffaele Scientific Institute, Ospedale San Raffaele
Milan,
ItalyActive - Recruiting
Italian Cohort Naive Antiretrovirals (ICONA)
Milano, 20124
ItalyActive - Recruiting
Modena HIV Cohort, Università degli Studi di Modena
Modena, 44100
ItalyActive - Recruiting
The ATHENA (AIDS Therapy Evaluation in the Netherlands) national observational HIV cohort, Stichting HIV Monitorin, AMC, University of Amsterdam
Amsterdam, 1105
NetherlandsActive - Recruiting
PISCIS Cohort Study, Germans Trias i Pujol University Hospital
Badalona, 08916
SpainActive - Recruiting
Swedish InfCare HIV Cohort, Karolinska University Hospital
Stockholm, 171 76
SwedenActive - Recruiting
Swiss HIV Cohort Study (SHCS), University Hospital Zurich
Zurich, 8091
SwitzerlandActive - Recruiting
Royal Free HIV Cohort Study, Royal Free Hospital
London, NW3 2 PF
United KingdomActive - Recruiting
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