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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.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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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
  • 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

    Recruiting

Other trials in France

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:

  1. to characterize the longitudinal association between asthma and cardiovascular (CV) risk assessed by the Framingham score,
  2. 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),
  3. 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.
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 groups in NCT06334705
Study groupRoleWhat they receive
participants can take part in any examinations they wishOtherNot 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.

  1. 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)
  1. Aortic pulse wave velocity

    comparison of aortic pulse wave velocity between asthmatics and non-asthmatics

    Measured: during clinical examination

  2. 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

  3. Soluble ST2

    comparison of a promising CV biomarker: soluble ST2 between asthmatics and non-asthmatics

    Measured: during clinical examination

  4. 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.

  1. First posted28 Mar 2024
  2. Study start15 Feb 2024
  3. Primary completion15 Feb 2027 (estimated)
  4. Study completion15 Feb 2028 (estimated)

Resources

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)
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

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.

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