Healthy Volunteer EGEA4 CohortNCT06334705
EGEA4 THE 30 YEAR FOLLOW UP OF THE EGEA STUDY
A study testing blood test, food collection, hair collection, calcium scan, etc. in people with Healthy Volunteer EGEA4 Cohort, run by Institut National de la Santé Et de la Recherche Médicale, France at 5 sites in France.
Trial summary
Cardiovascular (CV) diseases affect 523 million people worldwide, and are the leading cause of death, accounting for over 18 million deaths (around 30% of all deaths) every year. CV diseases account for around 45% of all deaths in Europe, or around 140,000 deaths a year in France. Read more about this study
- Who is it for?
- Ages 18 years and olderHealthy volunteers can take part
- Conditions the study is for
- Healthy Volunteer EGEA4 Cohort
- What is being tested?
- blood test, food collection, hair collection, calcium scan, etc.
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 1,000 participants
- Where
- 5 sitesFrance
- Study dates
- 15 Feb 2024to 15 Feb 2028
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
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
- Have participated in at least one of the previous EGEA surveys;
- to be affiliated to a social security scheme or to be a beneficiary of such a scheme.
Who cannot join
- Person deprived of liberty by judicial or administrative decision;
- Person subject to a legal protection measure (safeguard of justice, curatorship or guardianship).
Trial locations and contacts
5 sites in 1 country. Contact the study team or a site near you to ask about taking part.
5 sites in 1 country
France5 sites, 5 recruiting
- Recruiting
Centre Hospitalier Universitaire Grenoble Alpes
Grenoble, 38043
Bruno DEGANO, PhD, BDEGANO@chu-grenoble.fr
- Recruiting
Hopital de la Croix Rousse
Lyon, 69317
Gilles Mr DEVOUASSOUX, MD, gilles.devouassoux@chu-lyon.fr
- Recruiting
APHM
Marseille, 13000
Pascal CHANEZ, PhD, pascal.chanez@univ-amu.fr
- Recruiting
Hôpital Arnaud De Villeneuve
Montpellier, 34295
Pascal Mr DEMOLY, PHD, pascal.demoly@inserm.fr
- Recruiting
APHP - Hôpital Bichat Claude Bernard
Paris, 75018
Camille TAILLE, PHD, camille.taille@aphp.fr
About this study
Official title: EGEA4: the 30-year Follow-up of the EGEA Study : Study of Markers of Cardiovascular Risk in Asthmatic and Non-asthmatic
Cardiovascular (CV) diseases affect 523 million people worldwide, and are the leading cause of death, accounting for over 18 million deaths (around 30% of all deaths) every year. CV diseases account for around 45% of all deaths in Europe, or around 140,000 deaths a year in France. Asthma is one of the main non-communicable diseases, with a significant societal and individual burden, particularly in subjects suffering from severe asthma. The prevalence of asthma worldwide has risen rapidly over the past five decades, and now affects 272 million people worldwide, representing a prevalence of around 3.6%.
Asthma is often associated with multimorbidity. Allergic rhinitis, chronic sinusitis, sleep apnea syndrome, gastro-oesophageal reflux disease, obesity and hormonal disorders are among the most common conditions associated with asthma. More recently, other chronic conditions linked to asthma have been suggested, including CV diseases.
Read more
Although data from the literature in recent years suggest that asthma is associated with an increased risk of major CV events, the underlying mechanisms remain poorly understood. In particular, it is not known whether asthma and CV disease share common etiological processes, such as anthropometric parameters, lifestyle, social, environmental and/or genetic factors, or whether CV disease is a direct consequence of certain features of asthma, such as systemic inflammation or asthma treatments.
Our study is based on the hypothesis that the risk of CV events is increased in patients with asthma, which is supported by a growing body of scientific data.However, it remains to be determined to what extent this increased risk is a consequence of asthma or is linked to shared risk factors between asthma and CV health.
We hypothesize that asthma, and more specifically adult and moderate-to-severe asthma, are associated with early markers of CV risk. Furthermore, by providing a better understanding of the mechanisms involved in this association, we hypothesize that EGEA_30years may help to disentangle and prioritize actionable levers of life-threatening cardiovascular comorbidities in asthma.
Read the detailed description
Cardiovascular (CV) diseases, which include coronary heart disease and stroke, affect 523 million people worldwide and are the leading cause of death, accounting for over 18 million deaths (around 30% of all deaths) every year. CV diseases account for around 45% of all deaths in Europe, or around 140,000 deaths a year in France. Asthma is one of the main non-communicable diseases, with a significant societal and individual burden, particularly in subjects suffering from severe asthma. The worldwide prevalence of asthma has risen rapidly over the past five decades, and now affects 272 million people worldwide, representing a prevalence of around 3.6%, with considerable geographical variability.
Multimorbidity is common in asthma. Allergic rhinitis, chronic sinusitis, sleep apnea syndrome, gastroesophageal reflux disease, obesity and hormonal disorders are among the most common conditions linked to asthma.More recently, other chronic conditions linked to asthma have been suggested, including CV diseases.Although data from the literature in recent years suggest that asthma is associated with an increased risk of major CV events, the underlying mechanisms remain poorly understood. In particular, it is not known whether asthma and CV disease share common etiological processes, such as anthropometric parameters, lifestyle, social, environmental and/or genetic factors, or whether CV disease is a direct consequence of certain features of asthma, such as systemic inflammation or asthma treatments.
Our study is based on the hypothesis that the risk of CV events is increased in patients with asthma, which is supported by a growing body of scientific data.
However, it remains to be determined to what extent this increased risk is a consequence of asthma, or is linked to shared risk factors between asthma and CV health.We hypothesize that asthma, and more specifically adult and moderate-to-severe asthma, are associated with early markers of CV risk. Furthermore, by providing a better understanding of the mechanisms involved in this association, we hypothesize that EGEA_30years may help to disentangle and prioritize actionable levers of life-threatening cardiovascular comorbidities in asthma.
The main objectives of the EGEA4 study are:
- to characterize the longitudinal association between asthma and cardiovascular (CV) risk assessed by the Framingham score,
- study the association between asthma and other CV risk markers such as aortic pulse wave velocity (aPWV), validated predictive biomarkers of CV disease (NTproBNP, Troponin(I) hs), a promising CV biomarker (ST2 soluble) and coronary calcium score (CAC),
- to study the association between asthma control and severity and various markers of CV risk.
To meet the study's objectives, volunteers from the EGEA study, recruited between 1991-95 in 5 centers (Paris, Grenoble, Lyon, Montpellier, Marseille) and who have not dropped out, will be contacted to take part in a new follow-up (EGEA4).
The new follow-up will consist of a clinical visit to :
- administer a standardized face-to-face (or postal) questionnaire similar to that used in previous EGEA surveys to assess respiratory and allergic symptoms and diseases, the presence of chronic comorbidities, including CV events (e.g. stroke, arteriosclerosis, heart attack), quality of life, asthma control, lifestyle, diet (using a validated food frequency questionnaire to assess average dietary intake over the past 12 months), social and environmental factors (e.g. smoking and indoor environment) ;
- perform a clinical examination including :
- anthropometric measurements (height, weight, waist circumference and hip circumference) and impedance measurement
- blood pressure measurements;
- spirometry to measure pulmonary function;
- a one-minute chair-lift test to assess functional capacity;
- non-invasive measurement of an independent predictor of CV events, the aortic pulse wave velocity [aPWV], estimated by the speed of the pulse wave between the ankle and wrist;
- take a hair sample;
- take a blood sample; The visit will last 2h30 and will be carried out by clinical research staff trained in study procedures.
A second visit will be offered to volunteers at the Grenoble and Paris centers to take a non-invasive measurement assessed by CT scan (without injection), the Coronary Calcium Score (CAC), which is a predictor of the risk of cardiovascular events. If time permits, CAC can be measured during the first visit.
In addition, following the first visit, EGEA :
- equip the volunteer with an accelerometer (Actigraph). This accelerometer will be worn on the waist (or wrist) for one week;
- equip the volunteer with a passive pollution sensor (NO2). The volunteer will wear the sensor for one week. The sensor can be easily attached to a backpack/handbag.
- install the COBANET application on the volunteer's phone and explain how to use it. The purpose of this application is to collect information on the cleaning products used by the volunteer (product name and barcode), the frequency of use and the way in which these products are used (with or without protection, etc.);
- provide the volunteer with a kit containing the materials needed to collect stool samples
- create a "Nutrinet" account on the Nutrinet cohort platform, where the participant will log on in the days following the visit to complete three 24-hour dietary records.
- Conditions
- Healthy Volunteer EGEA4 Cohort
- Being tested
- blood test, food collection, hair collection, calcium scan, etc.
- Keywords
- Respiratory and cardiac health; Cohort; Epidemiology
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
blood test, food collection, hair collection, calcium scan, etc.Other
everything is specified during the phone call and in the consent form to be signed
| Study group | Role | What they receive |
|---|---|---|
| participants can take part in any examinations they wish | Other | Not described Receives: Other: blood test, food collection, hair collection, calcium scan, etc. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Framingham score variability between asthmatics and non-asthmatics
The primary endpoint will be the variability of the Framingham score between asthmatics and non-asthmatics to assess the association between asthma and cardiovascular (CV) risk.
Measured: during clinical examination
Secondary outcomes (4)
Aortic pulse wave velocity
comparison of aortic pulse wave velocity between asthmatics and non-asthmatics
Measured: during clinical examination
validated predictive biomarkers of CV disease (NTproBNP, Troponin(I) hs),
comparison of validated predictive biomarkers of CV disease (NTproBNP, Troponin(I) hs), between asthmatics and non-asthmatics
Measured: during clinical examination
Soluble ST2
comparison of a promising CV biomarker: soluble ST2 between asthmatics and non-asthmatics
Measured: during clinical examination
coronary calcium score
comparaison du score calcique coronaire entre les asthmatiques et non asthmatiques
Measured: during clinical examination
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted28 Mar 2024
- Study start15 Feb 2024
- Primary completion15 Feb 2027 (estimated)
- Study completion15 Feb 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Healthy Volunteer EGEA4 CohortStudies of the same condition, open and under way.
- More trials run by Institut National de la Santé Et de la Recherche Médicale, FranceThe 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
- Primary purpose
- Other
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 1,000 participants (estimated)
Sponsor and investigators
- Sponsor type
- Other government
- Collaborators
- APHP, Hospices Civils de Lyon, APHM, University Hospital, Grenoble, University Hospital, Montpellier
- Responsible party
- Sponsor
- Investigators
- Valérie Siroux, PHD, Principal investigator, Institut National de la Santé Et de la Recherche Médicale, France
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06334705
- Sponsor's protocol ID
- C22-11
- Other IDs
- 2022-A02312- 41
- Status last verified
- Sep 2025
- First submitted
- 18 Mar 2024
- Last updated
- 19 Sep 2025
- 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 19 Sep 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- EGEA4: the 30-year Follow-up of the EGEA Study : Study of Markers of Cardiovascular Risk in Asthmatic and Non-asthmatic
- ClinicalTrials.gov ID
- NCT06334705
- Acronym / sponsor ID
- C22-11
- Conditions
- Healthy Volunteer EGEA4 Cohort
- Keywords
- Respiratory and cardiac health; Cohort; Epidemiology
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 1,000 participants (estimated)
- Lead sponsor
- Institut National de la Santé Et de la Recherche Médicale, FranceOther government
- Collaborators
- APHP, Hospices Civils de Lyon, APHM, University Hospital, Grenoble, University Hospital, Montpellier
- Study start
- 15 Feb 2024 (actual)
- Primary completion
- 15 Feb 2027 (estimated)
- Study completion
- 15 Feb 2028 (estimated)
- First posted
- 28 Mar 2024 (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.
Cardiovascular (CV) diseases affect 523 million people worldwide, and are the leading cause of death, accounting for over 18 million deaths (around 30% of all deaths) every year. CV diseases account for around 45% of all deaths in Europe, or around 140,000 deaths a year in France. Asthma is one of the main non-communicable diseases, with a significant societal and individual burden, particularly in subjects suffering from severe asthma. The prevalence of asthma worldwide has risen rapidly over the past five decades, and now affects 272 million people worldwide, representing a prevalence of around 3.6%.
Asthma is often associated with multimorbidity. Allergic rhinitis, chronic sinusitis, sleep apnea syndrome, gastro-oesophageal reflux disease, obesity and hormonal disorders are among the most common conditions associated with asthma. More recently, other chronic conditions linked to asthma have been suggested, including CV diseases.
Although data from the literature in recent years suggest that asthma is associated with an increased risk of major CV events, the underlying mechanisms remain poorly understood. In particular, it is not known whether asthma and CV disease share common etiological processes, such as anthropometric parameters, lifestyle, social, environmental and/or genetic factors, or whether CV disease is a direct consequence of certain features of asthma, such as systemic inflammation or asthma treatments.
Our study is based on the hypothesis that the risk of CV events is increased in patients with asthma, which is supported by a growing body of scientific data.However, it remains to be determined to what extent this increased risk is a consequence of asthma or is linked to shared risk factors between asthma and CV health.
We hypothesize that asthma, and more specifically adult and moderate-to-severe asthma, are associated with early markers of CV risk. Furthermore, by providing a better understanding of the mechanisms involved in this association, we hypothesize that EGEA_30years may help to disentangle and prioritize actionable levers of life-threatening cardiovascular comorbidities in asthma.
Detailed description
Cardiovascular (CV) diseases, which include coronary heart disease and stroke, affect 523 million people worldwide and are the leading cause of death, accounting for over 18 million deaths (around 30% of all deaths) every year. CV diseases account for around 45% of all deaths in Europe, or around 140,000 deaths a year in France. Asthma is one of the main non-communicable diseases, with a significant societal and individual burden, particularly in subjects suffering from severe asthma. The worldwide prevalence of asthma has risen rapidly over the past five decades, and now affects 272 million people worldwide, representing a prevalence of around 3.6%, with considerable geographical variability.
Multimorbidity is common in asthma. Allergic rhinitis, chronic sinusitis, sleep apnea syndrome, gastroesophageal reflux disease, obesity and hormonal disorders are among the most common conditions linked to asthma.More recently, other chronic conditions linked to asthma have been suggested, including CV diseases.Although data from the literature in recent years suggest that asthma is associated with an increased risk of major CV events, the underlying mechanisms remain poorly understood. In particular, it is not known whether asthma and CV disease share common etiological processes, such as anthropometric parameters, lifestyle, social, environmental and/or genetic factors, or whether CV disease is a direct consequence of certain features of asthma, such as systemic inflammation or asthma treatments.
Our study is based on the hypothesis that the risk of CV events is increased in patients with asthma, which is supported by a growing body of scientific data.
However, it remains to be determined to what extent this increased risk is a consequence of asthma, or is linked to shared risk factors between asthma and CV health.We hypothesize that asthma, and more specifically adult and moderate-to-severe asthma, are associated with early markers of CV risk. Furthermore, by providing a better understanding of the mechanisms involved in this association, we hypothesize that EGEA_30years may help to disentangle and prioritize actionable levers of life-threatening cardiovascular comorbidities in asthma.
The main objectives of the EGEA4 study are:
- to characterize the longitudinal association between asthma and cardiovascular (CV) risk assessed by the Framingham score,
- study the association between asthma and other CV risk markers such as aortic pulse wave velocity (aPWV), validated predictive biomarkers of CV disease (NTproBNP, Troponin(I) hs), a promising CV biomarker (ST2 soluble) and coronary calcium score (CAC),
- to study the association between asthma control and severity and various markers of CV risk.
To meet the study's objectives, volunteers from the EGEA study, recruited between 1991-95 in 5 centers (Paris, Grenoble, Lyon, Montpellier, Marseille) and who have not dropped out, will be contacted to take part in a new follow-up (EGEA4).
The new follow-up will consist of a clinical visit to :
- administer a standardized face-to-face (or postal) questionnaire similar to that used in previous EGEA surveys to assess respiratory and allergic symptoms and diseases, the presence of chronic comorbidities, including CV events (e.g. stroke, arteriosclerosis, heart attack), quality of life, asthma control, lifestyle, diet (using a validated food frequency questionnaire to assess average dietary intake over the past 12 months), social and environmental factors (e.g. smoking and indoor environment) ;
- perform a clinical examination including :
- anthropometric measurements (height, weight, waist circumference and hip circumference) and impedance measurement
- blood pressure measurements;
- spirometry to measure pulmonary function;
- a one-minute chair-lift test to assess functional capacity;
- non-invasive measurement of an independent predictor of CV events, the aortic pulse wave velocity [aPWV], estimated by the speed of the pulse wave between the ankle and wrist;
- take a hair sample;
- take a blood sample; The visit will last 2h30 and will be carried out by clinical research staff trained in study procedures.
A second visit will be offered to volunteers at the Grenoble and Paris centers to take a non-invasive measurement assessed by CT scan (without injection), the Coronary Calcium Score (CAC), which is a predictor of the risk of cardiovascular events. If time permits, CAC can be measured during the first visit.
In addition, following the first visit, EGEA :
- equip the volunteer with an accelerometer (Actigraph). This accelerometer will be worn on the waist (or wrist) for one week;
- equip the volunteer with a passive pollution sensor (NO2). The volunteer will wear the sensor for one week. The sensor can be easily attached to a backpack/handbag.
- install the COBANET application on the volunteer's phone and explain how to use it. The purpose of this application is to collect information on the cleaning products used by the volunteer (product name and barcode), the frequency of use and the way in which these products are used (with or without protection, etc.);
- provide the volunteer with a kit containing the materials needed to collect stool samples
- create a "Nutrinet" account on the Nutrinet cohort platform, where the participant will log on in the days following the visit to complete three 24-hour dietary records.
Study design
- Primary purpose
- Other
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| participants can take part in any examinations they wish | Other | Other: blood test, food collection, hair collection, calcium scan, etc. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (2 listed)
- Have participated in at least one of the previous EGEA surveys;
- to be affiliated to a social security scheme or to be a beneficiary of such a scheme.
Key exclusion criteria (2 listed)
- Person deprived of liberty by judicial or administrative decision;
- Person subject to a legal protection measure (safeguard of justice, curatorship or guardianship).
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 test, food collection, hair collection, calcium scan, etc.everything is specified during the phone call and in the consent form to be signed | Other | participants can take part in any examinations they wish |
Primary outcome
Framingham score variability between asthmatics and non-asthmatics
Time frame: during clinical examination
The primary endpoint will be the variability of the Framingham score between asthmatics and non-asthmatics to assess the association between asthma and cardiovascular (CV) risk.
4 secondary outcomes
Aortic pulse wave velocity
Time frame: during clinical examination
validated predictive biomarkers of CV disease (NTproBNP, Troponin(I) hs),
Time frame: during clinical examination
Soluble ST2
Time frame: during clinical examination
coronary calcium score
Time frame: during clinical examination
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 19 Sep 2025.
- Related InfoLink provided by the sponsor.
- 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.
Valérie Siroux, PHD principal investigator
Institut National de la Santé Et de la Recherche Médicale, France
5 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing blood test, food collection, hair collection, calcium scan, etc. in people with Healthy Volunteer EGEA4 Cohort, run by Institut National de la Santé Et de la Recherche Médicale, France at 5 sites 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 2 inclusion and 2 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: looking for participants now, as of the sponsor's last update on 19 Sep 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 5 sites 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?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Valérie Siroux, PHD (0476549451, valerie.siroux@univ-grenoble-alpes.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Framingham score variability between asthmatics and non-asthmatics (time frame: during clinical examination). 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 19 Sep 2025.