Adult Patients Living With HIV (PLWHIV) With Confirmed Infection With SARS-CoV-2 Since 1st January 2020COVIDHIVNCT04361604
Clinical Characterisation Protocol for COVID-19 in People Living With HIV
An observational study of Adult Patients Living With HIV (PLWHIV) With Confirmed Infection With SARS-CoV-2 Since 1st January 2020, run by Assistance Publique - Hôpitaux de Paris at 1 site in France.
Trial summary
There is very little data so far to determine whether people living with HIV (PLWHIV) are at greater risk of COVID-19 acquisition or severe disease. HIV infection is associated with deficiencies in both humoral and cell-mediated immunity that could potentially alter the course and severity of common infections. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Adult Patients Living With HIV (PLWHIV) With Confirmed Infection With SARS-CoV-2 Since 1st January 2020
- What is being tested?
- Biological collection (patients co infected HIV Sras-CoV-2), Auto-questionnaires (patients co infected HIV Sras-CoV-2) and Qualitative interviews (in 40 patients : 20 with COVID-19 and 20 without COVID-19)
- How many people
- 270 participants
- Where
- 1 siteFrance
- Study dates
- Apr 2020to Oct 2020
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: This study will enroll 250 adult patients living with HIV (PLWHIV) with confirmed infection with SARS-CoV-2 since 1st January 2020. Recruitment of patients with Day 1 (enrolment) data is the priority. Twenty adult patients living with HIV (PLWHIV) without confirmed infection with SARS-CoV-2 will be enrolled only for qualitative interview. In order to be the most representative of PLHIV population and reach the number of patients to be included people who do not have social security affiliation or who are eligible may be included in the study. A derogation will be requested from the CPP for this.
Who may be able to join
- Patient living with HIV (PLWHIV)
- Patient with confirmed infection with SARS-CoV-2 since 1st January 2020 with and without criteria of hospitalisation.
- Inclusion criteria for the 20 patients without COVID19 (who will only realize the qualitative interview)
- Patient living with HIV (PLWHIV)
- Patient who did not have COVID-19
Who cannot join
- Confirmed diagnosis of another pathogen than SARS-CoV-2
- Refusal by participant, or appropriate representative.
- Being under guardianship or trusteeship mandate for future protection
- Participate to another study without consent of the promoter
- Patients less than 18 years old
- No Beneficiary or entitled to a social security scheme or state medical aid.
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- Exclusion criteria for the 20 patients without COVID19 (who will only realize the qualitative interview)
- Refusal by participant, or appropriate representative.
- Being under guardianship or trusteeship mandate for future protection
- Participate to another study without consent of the promoter
- Patients less than 18 years old
- No Beneficiary or entitled to a social security scheme or state medical aid.
Trial locations and contacts
1 site in 1 country.
France1 site
Department of Internal Medicine and Clinical Immunology of Professor Cécile Goujard
Le Kremlin-Bicêtre
Antoine Chéret, Dr, 0145212586, antoine.cheret@aphp.fr
About this study
There is very little data so far to determine whether people living with HIV (PLWHIV) are at greater risk of COVID-19 acquisition or severe disease. HIV infection is associated with deficiencies in both humoral and cell-mediated immunity that could potentially alter the course and severity of common infections. The investigators will study the correlation between clinical and immunovirological data. The singularity of this work is to have an in-depth immunovirological approach linked to the clinical characteristics in COVID-19 HIV co-infected patients. COVIDHIV is the only study to date to offer this combined approach in PLWHIV.
This protocol is a historical and prospective cohort study of PLWHIV presenting COVID-19 The primary objectives are to describe the course of COVID-19 disease in patients infected with HIV
Read the detailed description
Infectious diseases are a major cause of death worldwide. Recently a new coronavirus named SARS-CoV-2 has been identified as responsible of an initial epidemic respiratory disease, named COVID-19, in China since the 31 December 20191. COVID-19 has developed into a pandemic, with small chains of transmission in many countries and large chains resulting in extensive spread in a some countries, such as Italy, Iran, South Korea, and Japan 2 . Most countries are likely to have spread of COVID-19, at least in the early stages, before any mitigation measures have an impact and the COVID -19 epidemic is gradually taking hold in France 3.
There is very little data so far to determine whether people living with HIV (PLWHIV) are at greater risk of COVID-19 acquisition or severe disease. HIV infection is associated with deficiencies in both humoral and cell-mediated immunity that could potentially alter the course and severity of common infections. Although use of cART partially restores immune system, HIV-infected persons may remain at increased risk for morbidity associated with viral illnesses, especially if the ability to generate antigen-specific responses remains impaired 5. Additional factors, such as the high prevalence of smoking and chronic lung diseases among such patients, may further predispose HIV-infected patients to respiratory tract infections. Finally, they could be considered more vulnerable to SARS-CoV-2 infection because their immune systems are already under strain and cannot avoid the possibility of atypical presentations in these patients. Thus, we would like to implement a research as soon as possible concerning PLWHIV in order to adapt the care of these patients as fast as possible.
The investigator will study the correlation between clinical and immunovirological data. The singularity of this work is to have an in-depth immunovirological approach linked to the clinical characteristics in COVID-19 HIV co-infected patients. COVIDHIV is the only study to date to offer this combined approach in PLWHIV.
This protocol is a historical and prospective cohort study of PLWHIV presenting COVID-19
The primary objectives are to describe the course of COVID-19 disease in patients infected with HIV-1, and more specifically to:
- Describe the clinical and the biological features of the COVID-19 disease in PLWHIV
- Correlate the clinical characteristics with the immunovirological characteristics
- Describe the major complications and determine the factors associated with a worse evolution in PLWHIV
- Compare the data obtained to those of the similar works in progress in non PLWHIV
- Evaluate post-infectious clinical effects at a distance from the acute phase This study will enroll 250 adult patients living with HIV (PLWHIV) with confirmed infection with SARS-CoV-2 since 1st January 2020. Recruitment of patients with Day 1 (enrolment) data is the priority.
Twenty adult patients living with HIV (PLWHIV) without confirmed infection with SARS-CoV-2 will be enrolled only for qualitative interview.
In order to be the most representative of PLHIV population and reach the number of patients to be included people who do not have social security affiliation or who are eligible may be included in the study. A derogation will be requested from the CPP for this.
Research interventions include prospective collection of clinical data and biological sampling (blood, saliva, rectal swab (stool swab), urine, nasopharyngeal swab, conjonctival swab, semen (for 20 PLWHIV), CSF or other samples if indicated as part of standard care.). Auto-Questionnaires will be collected. Qualitative interviews will be realized in 40 patients (20 with COVID-19 and 20 without COVID-19)
- Being tested
- Biological collection (patients co infected HIV Sras-CoV-2), Auto-questionnaires (patients co infected HIV Sras-CoV-2), Qualitative interviews (in 40 patients : 20 with COVID-19 and 20 without COVID-19)
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Biological collection (patients co infected HIV Sras-CoV-2)Biological
Biological sampling (blood,saliva, tear urine, stool, respiratory tract, semen only for 20 patients, or other samples if indicated.)
Auto-questionnaires (patients co infected HIV Sras-CoV-2)Other
4 autoquestionnaires will be collected : HADS Hospital anxiety and depression scale, PCL-5 (post-traumatic stress disorder checklist version DSM-5), symptoms with the modified Justice Symptom Index PROQOL-HIV
Qualitative interviews (in 40 patients : 20 with COVID-19 and 20 without COVID-19)Other
Qualitative interviews will be realized in 40 patients (20 with COVID-19 and 20 without COVID-19)
| Study group | Role | What they receive |
|---|---|---|
| 250 Patients co infected HIV and SRAS-CoV2 | Cohort of Patient co infected HIV AND SRAS-CoV2 Receives: Biological: Biological collection (patients co infected HIV Sras-CoV-2); Other: Auto-questionnaires (patients co infected HIV Sras-CoV-2); Other: Qualitative interviews (in 40 patients : 20 with COVID-19 and 20 without COVID-19) | |
| 20 patients infected HIV without COVID-19 | Group of 20 comparative patients PLWHIV without COVID-19. This group will realise only the interview of the research. Receives: Other: Qualitative interviews (in 40 patients : 20 with COVID-19 and 20 without COVID-19) |
What is being measured
The primary outcome is the main question the study is designed to answer.
Describe the course of COVID-19 disease in patients infected with HIV,
Biological sample collection
Measured: 6 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted24 Apr 2020
- Study startApr 2020 (estimated)
- Primary completionOct 2020 (estimated)
- Study completionOct 2020 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Adult Patients Living With HIV (PLWHIV) With Confirmed Infection With SARS-CoV-2 Since 1st January 2020Studies of the same condition, open and under way.
- More trials run by Assistance Publique - Hôpitaux de ParisThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Other
- Enrolment
- 270 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Assistance Publique - Hôpitaux de Paris
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04361604
- Sponsor's protocol ID
- 2020-A00984-35
- Acronym
- COVIDHIV
- Status last verified
- Apr 2020
- First submitted
- 20 Apr 2020
- Last updated
- 24 Apr 2020
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 24 Apr 2020. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Clinical Characterisation Protocol for COVID-19 in People Living With HIV
- ClinicalTrials.gov ID
- NCT04361604
- Acronym / sponsor ID
- COVIDHIV / 2020-A00984-35
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 270 participants (estimated)
- Lead sponsor
- Assistance Publique - Hôpitaux de ParisUniversity, hospital or other
- Study start
- Apr 2020 (estimated)
- Primary completion
- Oct 2020 (estimated)
- Study completion
- Oct 2020 (estimated)
- First posted
- 24 Apr 2020 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
There is very little data so far to determine whether people living with HIV (PLWHIV) are at greater risk of COVID-19 acquisition or severe disease. HIV infection is associated with deficiencies in both humoral and cell-mediated immunity that could potentially alter the course and severity of common infections. The investigators will study the correlation between clinical and immunovirological data. The singularity of this work is to have an in-depth immunovirological approach linked to the clinical characteristics in COVID-19 HIV co-infected patients. COVIDHIV is the only study to date to offer this combined approach in PLWHIV.
This protocol is a historical and prospective cohort study of PLWHIV presenting COVID-19 The primary objectives are to describe the course of COVID-19 disease in patients infected with HIV
Detailed description
Infectious diseases are a major cause of death worldwide. Recently a new coronavirus named SARS-CoV-2 has been identified as responsible of an initial epidemic respiratory disease, named COVID-19, in China since the 31 December 20191. COVID-19 has developed into a pandemic, with small chains of transmission in many countries and large chains resulting in extensive spread in a some countries, such as Italy, Iran, South Korea, and Japan 2 . Most countries are likely to have spread of COVID-19, at least in the early stages, before any mitigation measures have an impact and the COVID -19 epidemic is gradually taking hold in France 3.
There is very little data so far to determine whether people living with HIV (PLWHIV) are at greater risk of COVID-19 acquisition or severe disease. HIV infection is associated with deficiencies in both humoral and cell-mediated immunity that could potentially alter the course and severity of common infections. Although use of cART partially restores immune system, HIV-infected persons may remain at increased risk for morbidity associated with viral illnesses, especially if the ability to generate antigen-specific responses remains impaired 5. Additional factors, such as the high prevalence of smoking and chronic lung diseases among such patients, may further predispose HIV-infected patients to respiratory tract infections. Finally, they could be considered more vulnerable to SARS-CoV-2 infection because their immune systems are already under strain and cannot avoid the possibility of atypical presentations in these patients. Thus, we would like to implement a research as soon as possible concerning PLWHIV in order to adapt the care of these patients as fast as possible.
The investigator will study the correlation between clinical and immunovirological data. The singularity of this work is to have an in-depth immunovirological approach linked to the clinical characteristics in COVID-19 HIV co-infected patients. COVIDHIV is the only study to date to offer this combined approach in PLWHIV.
This protocol is a historical and prospective cohort study of PLWHIV presenting COVID-19
The primary objectives are to describe the course of COVID-19 disease in patients infected with HIV-1, and more specifically to:
- Describe the clinical and the biological features of the COVID-19 disease in PLWHIV
- Correlate the clinical characteristics with the immunovirological characteristics
- Describe the major complications and determine the factors associated with a worse evolution in PLWHIV
- Compare the data obtained to those of the similar works in progress in non PLWHIV
- Evaluate post-infectious clinical effects at a distance from the acute phase This study will enroll 250 adult patients living with HIV (PLWHIV) with confirmed infection with SARS-CoV-2 since 1st January 2020. Recruitment of patients with Day 1 (enrolment) data is the priority.
Twenty adult patients living with HIV (PLWHIV) without confirmed infection with SARS-CoV-2 will be enrolled only for qualitative interview.
In order to be the most representative of PLHIV population and reach the number of patients to be included people who do not have social security affiliation or who are eligible may be included in the study. A derogation will be requested from the CPP for this.
Research interventions include prospective collection of clinical data and biological sampling (blood, saliva, rectal swab (stool swab), urine, nasopharyngeal swab, conjonctival swab, semen (for 20 PLWHIV), CSF or other samples if indicated as part of standard care.). Auto-Questionnaires will be collected. Qualitative interviews will be realized in 40 patients (20 with COVID-19 and 20 without COVID-19)
Study design
- Observational model
- Cohort
- Time perspective
- Other
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| 250 Patients co infected HIV and SRAS-CoV2 | – | Biological: Biological collection (patients co infected HIV Sras-CoV-2), Other: Auto-questionnaires (patients co infected HIV Sras-CoV-2), Other: Qualitative interviews (in 40 patients : 20 with COVID-19 and 20 without COVID-19)Cohort of Patient co infected HIV AND SRAS-CoV2 |
| 20 patients infected HIV without COVID-19 | – | Other: Qualitative interviews (in 40 patients : 20 with COVID-19 and 20 without COVID-19)Group of 20 comparative patients PLWHIV without COVID-19. This group will realise only the interview of the research. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- This study will enroll 250 adult patients living with HIV (PLWHIV) with confirmed infection with SARS-CoV-2 since 1st January 2020. Recruitment of patients with Day 1 (enrolment) data is the priority. Twenty adult patients living with HIV (PLWHIV) without confirmed infection with SARS-CoV-2 will be enrolled only for qualitative interview. In order to be the most representative of PLHIV population and reach the number of patients to be included people who do not have social security affiliation or who are eligible may be included in the study. A derogation will be requested from the CPP for this.
Key inclusion criteria (5 listed)
- Patient living with HIV (PLWHIV)
- Patient with confirmed infection with SARS-CoV-2 since 1st January 2020 with and without criteria of hospitalisation.
- Inclusion criteria for the 20 patients without COVID19 (who will only realize the qualitative interview)
- Patient living with HIV (PLWHIV)
- Patient who did not have COVID-19
Key exclusion criteria (12 listed)
- Confirmed diagnosis of another pathogen than SARS-CoV-2
- Refusal by participant, or appropriate representative.
- Being under guardianship or trusteeship mandate for future protection
- Participate to another study without consent of the promoter
- Patients less than 18 years old
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Biological collection (patients co infected HIV Sras-CoV-2)Biological sampling (blood,saliva, tear urine, stool, respiratory tract, semen only for 20 patients, or other samples if indicated.) | Biological | 250 Patients co infected HIV and SRAS-CoV2 |
| Auto-questionnaires (patients co infected HIV Sras-CoV-2)4 autoquestionnaires will be collected : HADS Hospital anxiety and depression scale, PCL-5 (post-traumatic stress disorder checklist version DSM-5), symptoms with the modified Justice Symptom Index PROQOL-HIV | Other | 250 Patients co infected HIV and SRAS-CoV2 |
| Qualitative interviews (in 40 patients : 20 with COVID-19 and 20 without COVID-19)Qualitative interviews will be realized in 40 patients (20 with COVID-19 and 20 without COVID-19) | Other | 20 patients infected HIV without COVID-19, 250 Patients co infected HIV and SRAS-CoV2 |
Primary outcome
Describe the course of COVID-19 disease in patients infected with HIV,
Time frame: 6 months
Biological sample collection
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 24 Apr 2020.
- Individual participant dataSharing planned: No
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Department of Internal Medicine and Clinical Immunology of Professor Cécile Goujard
Le Kremlin-Bicêtre, France
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Adult Patients Living With HIV (PLWHIV) With Confirmed Infection With SARS-CoV-2 Since 1st January 2020, run by Assistance Publique - Hôpitaux de Paris at 1 site in France.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 5 inclusion and 12 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 24 Apr 2020. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Each site lists its own contact: choose the nearest one under Trial locations. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Describe the course of COVID-19 disease in patients infected with HIV, (time frame: 6 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 Apr 2020.