Hiv InfectionANRS EP 52NCT01899196
Epicardial Adipose Tissue And Coronary Risk In HIV-Infected Patients
A study testing blood sampling, in people with Hiv Infection, run by ANRS, Emerging Infectious Diseases at 1 site in France.
Trial summary
Protocol date and version RCB Id : 2013-A00547-38 Etude ANRS EP 52 PIECVIH Title of Study: EPICARDIAL ADIPOSE TISSUE AND CORONARY RISK IN HIV-INFECTED PATIENTS Short title - PIECVIH study Sponsor French National Institute for Health and Medical Research - French national agency for research on AIDS and viral hepatitis… Read more about this study
- Who is it for?
- Ages 18 years and olderHealthy volunteers can take part
- Conditions the study is for
- Hiv Infection
- What is being tested?
- blood sampling,
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 24 participants
- Where
- 1 siteFrance
- Study dates
- Jul 2013to Mar 2016
- Phase
- Interventional
- 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
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- VIH + GROUP:
- Men or women > 18 years old, HIV1 + for more than 6 months
- Planned first cardiac surgery for CABG
- VIH - GROUP:
- Men or women > 18 years old,
- Planned first cardiac surgery for CABG
Who cannot join
- History of cardiac surgery
Trial locations and contacts
1 site in 1 country.
About this study
Official title: EPICARDIAL ADIPOSE TISSUE AND CORONARY RISK IN HIV-INFECTED PATIENTS
Protocol date and version RCB Id : 2013-A00547-38
Etude ANRS EP 52 PIECVIH Title of Study: EPICARDIAL ADIPOSE TISSUE AND CORONARY RISK IN HIV-INFECTED PATIENTS
Read more
Short title - PIECVIH study
Sponsor French National Institute for Health and Medical Research - French national agency for research on AIDS and viral hepatitis (Inserm-ANRS)
Coordinating Investigator Pr Franck BOCCARA Service de Cardiologie, Hôpital St Antoine INSERM UMRS 938 Paris, UPMC, Institut hospitalo-Universitaire- Institute of Cardiometabolism and Nutrition (IHU-ICAN) 184, rue du Faubourg Saint-Antoine 75571 PARIS Cedex 12 Tél. : 01 49 28 24 49 - Fax : 01 49 28 26 83 Courriel : franck.boccara@sat.aphp.fr
Participating country: France
Objectives Principal objective To compare the inflammatory profile of the epicardial adipose tissue (EAT) between people living with and without HIVwho present with coronary heart disease and will undergo a coronary artery bypass graft (CABG)
Secondary objectives
- To compare the volume of EAT between people living with and without HIV who present with coronary heart disease
- To evaluate the relationship between the abnormalities of the expression profiles of the adipocytokines and cytokines with the atherosclerotic lesions.
- To evaluate the relationship between the abnormalities of the expression profiles of the adipocytokines and cytokines of the EAT with the circulating levels and metabolic parameters.
- To compare the histological and inflammatory profiles of the EAT with the subcutaneous adipose tissue for each patient individually.
Methodology multicentric, comparative study
Estimated enrollment 31 participants in total
- st group of- 15 people living with HIV undergoing CABG (coronary heart disease HIV+ group)
- nd group of- 16 people without HIV- undergoing CABG (coronary heart disease HIV- group) People without HIV-will be matched to people living with HIV+ by : age (± 5 years) and sex Outcomes
Primary outcome:
Comparative analysis of the inflammatory profile of the EAT : expression profile of the pro and anti inflammatory cytokines and adipokines within the EAT in both groups of participants : coronary heart disease HIV+ and HIV- groups
Secondary outcomes :
- Determination of the EAT volume by echocardiography and cardiac scanner for both groups
- Macroscopic profile of the EAT : adipocytes, fibrosis, endothelial cell density)
- RT-PCR analyses : renin, adiponectine, PPARɣ
- Comparatison of the inflammatory and macroscopic profiles between the EAT and the subcutaneous adipose tissue in the two groups by ARN messagers analysis.
Eligibility Inclusion criteria HIV+ group
- Men or women above the age of 18 years old, HIV1 seropositive for more than 6 months
- Individual undergoing, for the first time, cardiac surgery for CABG
- Affiliated with a social security regimen (the AME is not a social security regimen)
- Signed the consent form
HIV- group
- Men or women above the age of 18 years old, HIV seronegative
- Individuals undergoing, for the first time, cardiac surgery for CABG
- Affiliated with a social security regimen (the AME is not a social security regimen)
- Signed the consent form
Non-inclusion criteria History of surgery for CBAG and/or congenital heart defect- being under the tutorship or guardianship of the state or in custody of the justice system.
Statistical methods Categorical variables will be compared using Fisher's exact test. Continuous variables will be compared using the Student's t-test (parametric) and the Wilcoxon-Mann-Whitney test (non-parametric) as appropriate considering the data distribution. (statistical analysis software STATA 11 (StataCorp, Texas, USA))
Provisional study planning and timetable Study start date: July 2013 Enrollment period: 32 months Subject participation duration: 24 hours Total study duration: 32 months Estimated study completion date: end of March 2016
- Conditions
- Hiv Infection
- Being tested
- blood sampling,
- Keywords
- Cardiac surgery
- Medical subject headings
- HIV Infections
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
blood sampling,Biological
| Study group | Role | What they receive |
|---|---|---|
| no Arm | Other | Not described Receives: Biological: blood sampling, |
What is being measured
The primary outcome is the main question the study is designed to answer.
comparison of the inflammatory profile of the epicardial adipose (EAT) tissue between HIV-infected and uninfected patients undergoing cardiac surgery for coronary artery bypass graft (CABG)
Measured: day 1
Secondary outcomes (4)
comparison the volume of EAT between HIV-infected and uninfected patients undergoing cardiac surgery
Measured: day 1
Evaluation of the relations between the adipocytokines and cytokines profile in the EAT and in the systemic circulation.
Measured: day 1
Comparison of the histological and inflammatory profiles of the EAT and the subcutaneous adipose tissue of each patients.
Measured: day 1
Evaluation of the relations between the adipocytokines and cytokines profile in the EAT and coronary artery lesions.
Measured: day 1
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted15 Jul 2013 (estimated)
- Study startJul 2013
- Primary completionMar 2016
- Study completionMar 2016
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Hiv InfectionStudies of the same condition, open and under way.
- More trials run by ANRS, Emerging Infectious DiseasesThe 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
- Interventional
- Phase
- Phase N/A
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 24 participants (actual)
Sponsor and investigators
- Lead sponsor
- ANRS, Emerging Infectious Diseases
- Sponsor type
- Other government
- Responsible party
- Sponsor
- Investigators
- Pascal LEPRINCE, Principal investigator, Hôpital La Pitié Salpétrière Paris
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01899196
- Sponsor's protocol ID
- ANRS EP 52 PIECVIH
- Acronym
- ANRS EP 52
- Status last verified
- Jul 2016
- First submitted
- 2 Jul 2013
- Last updated
- 6 Jul 2016
- Results posted
- No
- Data monitoring committee
- No
Study at a glance
From the registry record, last updated by the sponsor on 6 Jul 2016. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- EPICARDIAL ADIPOSE TISSUE AND CORONARY RISK IN HIV-INFECTED PATIENTS
- ClinicalTrials.gov ID
- NCT01899196
- Acronym / sponsor ID
- ANRS EP 52 / ANRS EP 52 PIECVIH
- Conditions
- Hiv Infection
- Keywords
- Cardiac surgery
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 24 participants (actual)
- Lead sponsor
- ANRS, Emerging Infectious DiseasesOther government
- Study start
- Jul 2013
- Primary completion
- Mar 2016 (actual)
- Study completion
- Mar 2016 (actual)
- First posted
- 15 Jul 2013 (estimated)
- 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.
Protocol date and version RCB Id : 2013-A00547-38
Etude ANRS EP 52 PIECVIH Title of Study: EPICARDIAL ADIPOSE TISSUE AND CORONARY RISK IN HIV-INFECTED PATIENTS
Short title - PIECVIH study
Sponsor French National Institute for Health and Medical Research - French national agency for research on AIDS and viral hepatitis (Inserm-ANRS)
Coordinating Investigator Pr Franck BOCCARA Service de Cardiologie, Hôpital St Antoine INSERM UMRS 938 Paris, UPMC, Institut hospitalo-Universitaire- Institute of Cardiometabolism and Nutrition (IHU-ICAN) 184, rue du Faubourg Saint-Antoine 75571 PARIS Cedex 12 Tél. : 01 49 28 24 49 - Fax : 01 49 28 26 83 Courriel : franck.boccara@sat.aphp.fr
Participating country: France
Objectives Principal objective To compare the inflammatory profile of the epicardial adipose tissue (EAT) between people living with and without HIVwho present with coronary heart disease and will undergo a coronary artery bypass graft (CABG)
Secondary objectives
- To compare the volume of EAT between people living with and without HIV who present with coronary heart disease
- To evaluate the relationship between the abnormalities of the expression profiles of the adipocytokines and cytokines with the atherosclerotic lesions.
- To evaluate the relationship between the abnormalities of the expression profiles of the adipocytokines and cytokines of the EAT with the circulating levels and metabolic parameters.
- To compare the histological and inflammatory profiles of the EAT with the subcutaneous adipose tissue for each patient individually.
Methodology multicentric, comparative study
Estimated enrollment 31 participants in total
- st group of- 15 people living with HIV undergoing CABG (coronary heart disease HIV+ group)
- nd group of- 16 people without HIV- undergoing CABG (coronary heart disease HIV- group) People without HIV-will be matched to people living with HIV+ by : age (± 5 years) and sex Outcomes
Primary outcome:
Comparative analysis of the inflammatory profile of the EAT : expression profile of the pro and anti inflammatory cytokines and adipokines within the EAT in both groups of participants : coronary heart disease HIV+ and HIV- groups
Secondary outcomes :
- Determination of the EAT volume by echocardiography and cardiac scanner for both groups
- Macroscopic profile of the EAT : adipocytes, fibrosis, endothelial cell density)
- RT-PCR analyses : renin, adiponectine, PPARɣ
- Comparatison of the inflammatory and macroscopic profiles between the EAT and the subcutaneous adipose tissue in the two groups by ARN messagers analysis.
Eligibility Inclusion criteria HIV+ group
- Men or women above the age of 18 years old, HIV1 seropositive for more than 6 months
- Individual undergoing, for the first time, cardiac surgery for CABG
- Affiliated with a social security regimen (the AME is not a social security regimen)
- Signed the consent form
HIV- group
- Men or women above the age of 18 years old, HIV seronegative
- Individuals undergoing, for the first time, cardiac surgery for CABG
- Affiliated with a social security regimen (the AME is not a social security regimen)
- Signed the consent form
Non-inclusion criteria History of surgery for CBAG and/or congenital heart defect- being under the tutorship or guardianship of the state or in custody of the justice system.
Statistical methods Categorical variables will be compared using Fisher's exact test. Continuous variables will be compared using the Student's t-test (parametric) and the Wilcoxon-Mann-Whitney test (non-parametric) as appropriate considering the data distribution. (statistical analysis software STATA 11 (StataCorp, Texas, USA))
Provisional study planning and timetable Study start date: July 2013 Enrollment period: 32 months Subject participation duration: 24 hours Total study duration: 32 months Estimated study completion date: end of March 2016
Study design
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| no Arm | Other | Biological: blood sampling, |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (6 listed)
- Men or women > 18 years old, HIV1 + for more than 6 months
- Planned first cardiac surgery for CABG
- Men or women > 18 years old,
- Planned first cardiac surgery for CABG
Key exclusion criteria (1 listed)
- History of cardiac surgery
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 |
|---|---|---|
| blood sampling, | Biological | no Arm |
Primary outcome
comparison of the inflammatory profile of the epicardial adipose (EAT) tissue between HIV-infected and uninfected patients undergoing cardiac surgery for coronary artery bypass graft (CABG)
Time frame: day 1
4 secondary outcomes
comparison the volume of EAT between HIV-infected and uninfected patients undergoing cardiac surgery
Time frame: day 1
Evaluation of the relations between the adipocytokines and cytokines profile in the EAT and in the systemic circulation.
Time frame: day 1
Comparison of the histological and inflammatory profiles of the EAT and the subcutaneous adipose tissue of each patients.
Time frame: day 1
Evaluation of the relations between the adipocytokines and cytokines profile in the EAT and coronary artery lesions.
Time frame: day 1
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 6 Jul 2016.
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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.
Pascal LEPRINCE principal investigator
Hôpital La Pitié Salpétrière Paris
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing blood sampling, in people with Hiv Infection, run by ANRS, Emerging Infectious Diseases 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 6 inclusion and 1 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: finished, as of the sponsor's last update on 6 Jul 2016. 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?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
comparison of the inflammatory profile of the epicardial adipose (EAT) tissue between HIV-infected and uninfected patients undergoing cardiac surgery for coronary artery bypass graft (CABG) (time frame: day 1). 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 6 Jul 2016.