COHIVE: Coronavirus (COVID-19) Outcomes in HIV Evaluation in Resource Limited Settings
- Conditions
- HIV-infection/AidsCoronavirus Infection
- Registration Number
- NCT04371835
- Lead Sponsor
- Kirby Institute
- Brief Summary
COHIVE is an observational cohort nested in four antiretroviral therapy research studies (ADVANCE - NCT03122262; D²EFT - NCT03017872; DolPHIN2 - NCT03249181 and NAMSAL-ANRS12313 - NCT02777229). COHIVE will include participants who are possible COVID-19 cases with symptoms or confirmed COVID-19 cases, and participants who agree to have a serology testing for SARS-CoV-2 regardless of COVID-19 history.
- Detailed Description
COHIVE is an observational cohort study nested within four parent open label randomised clinical trials of first- and second-line antiretroviral therapies (ADVANCE - NCT03122262; D²EFT - NCT03017872; DolPHIN2 - NCT03249181 and NAMSAL-ANRS12313 - NCT02777229). COHIVE objective is to study the occurrence and outcomes of COVID-19 in people living with HIV across a variety of clinical settings. Taken together, these pivotal trials provide an established population and encompass a range of HIV therapies, HIV populations, and geographic regions to capture the full spectrum of these global public health emergency as it pertains to people living with HIV.
The sample will include participants who are possible symptomatic or confirmed COVID-19 cases, and participants who agree to enrol in the SARS-CoV-2 seroprevalence cohort (regardless of SARS-CoV-2 infection). Approximately 2,500 participants are enrolled in these 4 studies.
Enrolment into COHIVE substudy is voluntary and optional for participants in ADVANCE, D²EFT, DolPHIN2 and NAMSAL studies. Parameters relevant to COHIVE substudy including demographics, arm of randomised ART, medical and HIV history, immunological and virological results, adverse events at required time points will be collected as part of parent studies. Substudy specific assessments performed at baseline include optional sample collection for SARS-CoV-2 RT-PCR and serology; for the possible symptomatic or confirmed COVID-19 cases, the management of the patients, diagnostic test results, and outcomes, will be collected.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 596
- ≥ 18 years old.
- Either: i) Meet local testing criteria for COVID-19, or present with symptoms that in the opinion of the investigator are consistent with COVID-19 and do not have an alternative explanation, or have tested elsewhere and found positive for COVID-19; OR ii) Agree for serology testing for SARS-CoV2, regardless of history of COVID-19.
- Have signed the informed consent of one of the parent study.
- Give informed consent to the COHIVE substudy.
- Refuse to participate in the COHIVE substudy.
- Any condition which would place the participant at risk if they participated.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Clinical outcomes of symptomatic COVID-19 in PLWH At Month 3 To characterise the clinical outcomes of symptomatic COVID-19 in PLWH, assessing the outcomes of patients including the percentage of patients who are fully recovered, required hospitalisation, developed severe illness (ICU admission or equivalent) or died.
Clinical features of symptomatic COVID-19 in people living with HIV (PLWH) At baseline To characterise the clinical features of symptomatic COVID-19 in PLWH (cardio-respiratory and other clinical signs or symptoms), described overall and by HIV and comorbid disease factors including pregnancy status.
- Secondary Outcome Measures
Name Time Method Seroprevalence of COVID-19 in all parent study participants Through study completion, an average of one year To determine seroprevalence of COVID-19 in all parent study participants regardless of COVID-19 history.
Trial Locations
- Locations (15)
Hospital G de Agudos JM Ramos Mejia
🇦🇷Buenos Aires, Ciudad De Buenos Aires, Argentina
Central Hospital of Yaoundé
🇨🇲Yaoundé, Cameroon
Laboratório de Pesquisa Clinica Em Hiv/Aids - Instituto Nacional de Infectologia - Fiocruz
🇧🇷Rio de Janeiro, Brazil
Cité Verte Hospital
🇨🇲Yaoundé, Cameroon
Hôpital Militaire de Région N°1
🇨🇲Yaoundé, Cameroon
CART CRS, VHS Hospital
🇮🇳Chennai, Tamil Nadu, India
Univerity of Malaya Medical Centre
🇲🇾Kuala Lumpur, Malaysia
Institute of Human Virology, Nigeria (IHVN)
🇳🇬Abuja, Nigeria
Desmond Tutu HIV Foundation
🇿🇦Cape Town, South Africa
Perinatal HIV Research Unit (PHRU)
🇿🇦Johannesburg, South Africa
Clinical HIV Research Unit (CHRU), Wits Health Consotium (Pty) Ltd
🇿🇦Johannesburg, South Africa
Ezintsha
🇿🇦Parktown, South Africa
HIV-NAT (The HIV Netherlands Australia Thailand Research Collaboration), Thai Red Cross AIDS Research Centre
🇹🇭Bangkok, Thailand
Infectious Diseases Institute
🇺🇬Kampala, Uganda
University of Zimbabwe Clinical Research Centre
🇿🇼Harare, Zimbabwe