ClinicalTrials.gg
Not yet recruitingNCT07780630BRISEUpdated Aug 21, 2026

Creation of a Biological Collection of BRonchiaI and Pulmonary Tissues From Surgical wastE

An observational study in COPD (Chronic Obstructive Pulmonary Disease), Asthma (Diagnosis) and Safe Volunteers, sponsored by University Hospital, Bordeaux. Not yet recruiting at 1 site in France. Open to participants aged 1 Year to 80 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-08-21.

Sponsored by University Hospital, Bordeaux · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
650
Ages
1 Year to 80 Years
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-12

Among 15 studies in Pulmonary Disease, Chronic Obstructive by University Hospital, Bordeaux — 2 open to participants now, 3 under way, none of them phase 3. Pulmonary Disease, Chronic Obstructive · University Hospital, Bordeaux.

Started
2026
with 1 other
Observational
3 of 15
1 open now
Registered
14th of 15
by date

Among the 15 studies in Pulmonary Disease, Chronic Obstructive by University Hospital, Bordeaux, this one is one of 2 that started in 2026, is one of 3 observational ones, and was the 14th registered.

By phase

15 studies; the count open now beside each. This study's row is marked.

No phase8 · 1 open
Observationalthis study3 · 1 open
Other kind1 · 0 open
Phase 21 · 0 open
Phase 31 · 0 open
Phase 41 · 0 open

By the year they started

First in 2004; this study’s year is marked. 2 started in 2026.

Size and results

Median enrollment 42 across the 10 interventional studies, 151 across the 4 observational. Of the 11 that completed or were terminated, 0 (0%) have results posted.

Watch this landscapeDownload CSVWith an account: a weekly mail of what changed among 15 studies in Pulmonary Disease, Chronic Obstructive by University Hospital, Bordeaux, or all of them as a file.
02

Study summary

The biological samples and associated data will facilitate the successful implementation of the research collaboration between Bordeaux University Hospital and the University of Bordeaux on the pathophysiology of bronchopulmonary diseases. In the longer term, this research could lead to the discovery of new therapeutic targets for asthma, chronic obstructive pulmonary disease (COPD), pulmonary hypertension, and acute respiratory distress syndrome.

Read the detailed description

Bronchial obstructive diseases, such as asthma and chronic obstructive pulmonary disease (COPD), are very common and pose a major public health problem. Asthma affects about 7% and COPD affects 3% of the population in France. In children, the prevalence of asthma is even higher and can reach 15 to 20%. These two diseases are responsible for many hospitalizations and emergency room stays. While asthma mortality has been considerably reduced over the last 30 years, COPD mortality continues to increase to reach the 3rd leading cause of mortality. In COPD, pulmonary hypertension (PH) is a common comorbidity that increases mortality.

In each of these diseases, bronchial remodeling occurs from the beginning of the disease, including in children. Long considered an abnormal process of tissue repair after inflammation, it is now considered to be concomitant with bronchial inflammation. It conditions the prognosis of the disease but its pathophysiological processes remain largely unknown.

In asthma, bronchial remodeling is characterized by epithelial abrasion, pseudo-thickening of the basement membrane, bronchial fibrosis, hypertrophy of the submucosal glands, neoangiogenesis and increased bronchial smooth muscle mass. In the laboratory, the investigators have shown that the mechanisms responsible for this increase in bronchial smooth muscle mass are complex and involve in particular the mitochondria of bronchial smooth muscle in both adults and children.

In COPD, bronchial remodeling is characterized by epithelial metaplasia, hypertrophy of the submucosal glands, peribronchial fibrosis, and increased bronchial smooth muscle mass.

In the laboratory, it has been shown that fibrocytes are involved in peribronchial fibrosis. In addition, at the level of the lung parenchyma, there is a destruction of the distal airway spaces responsible for pulmonary emphysema. In some COPD patients, pulmonary hypertension occurs and is accompanied by remodeling of the pulmonary arteries with thickening of the media, and pulmonary arterial fibrosis.

Apart from adult acute respiratory distress syndrome (ARDS), it is an acute disease with a high risk of secondary pulmonary fibrosis. This is characterized by alveolar fibrosis with a proliferation of fibroblasts.

The COBRA cohort (Bronchial Obstruction and Asthma Cohort), sponsored by INSERM, makes it possible to obtain, with the consent of patients, bronchial tissues, blood, sputum of adult asthma or COPD patients from bronchial biopsies and brushing, Boncho-Alveolar lavage (BAL) obtained during bronchial fiberscopies, blood, sputum.

The results of experiments on asthmatic tissues should be compared with those from non-asthmatic subjects. In adults, these tissues come from surgical waste during lobectomy/pneumonectomy or lung transplantation. In children, these tissues are collected as part of the ARISE, BIRDIES, VIRCHILLD and more recently ICEBERG protocols (all promoted by the Bordeaux University Hospital) which make it possible to perform bronchial brushing and/or bronchial biopsies during bronchial fiberscopy, nasal brushing, surgical waste during a lobectomy and blood. These tissues thus make it possible to cultivate these same smooth muscle cells and bronchial epithelial cells. Adult surgical waste also makes it possible to grow cells from COPD patients at different stages of severity. They also make it possible to extract and culture other cell types involved in the pathophysiology of COPD such as fibrocytes, pneumocytes, endothelial and pulmonary vascular smooth muscle cells and other inflammatory cells such as lymphocytes, neutrophils, macrophages, mast cells, etc. This is because the immune cells in lung tissue are different from those in circulating blood. All of these cell types can be cultured in organoid models of bronchi, alveoli, submucosal glands, or even pulmonary vessels.

Depending on the respiratory function of the operated patients, measured pre-operatively, the bronchial/parenchymal and arterial pulmonary tissues may reflect a "healthy" tissue (non-asthmatic, non-COPD) or mild to severe COPD with or without pulmonary hypertension.

03

Conditions studied

  • COPD (Chronic Obstructive Pulmonary Disease)
  • Asthma (Diagnosis)
  • Safe Volunteers
04

Who can participate

Ages eligible
1 Year to 80 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

The population includes male and female participants of all ages (adults and children) who are undergoing or require specific thoracic or bronchial procedures, sputum, nasal brushing, blood as part of clinical care or research. These procedures are conducted under the auspices of Bordeaux University Hospital (e.g., ARISE, BIRDIES, ICEBERG, VIRCHILLD) or Inserm (e.g., COBRA).

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Male or female
  • Adult or children
  • Having required or necessitating, in the context of care or research involving the human person promoted by the Bordeaux University Hospital (ARISE, BIRDIES, ICEBERG, VIRCHILLD) or by Inserm (COBRA), either thoracic surgery such as lobectomy, pneumonectomy or lung transplantation in the Thoracic Surgery Department of the Haut Lévêque Hospital, or bronchial fiberscopy with and/or bronchial brushing and/or BAL at the children's hospital of the Pellegrin Hospital or at the Haut Lévêque Hospital.
  • Having received or, for children whose holders of parental authority have received, an information note with the possibility of opposition in accordance with the MR004 (French law - Commission Nationale de l'Informatique et des Libertés (CNIL))

Exclusion criteria

Exclusion Criteria:

  • Patient or holder of parental authority for children who have expressed their opposition to participation in the research
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Biopsy and archival tissue

A biopsy takes a small piece of tissue to examine. “Archival tissue” is a sample already taken, for example at diagnosis, and kept by the hospital.

Whether a stored sample will do depends on when it was taken, how much there is and what the study needs. Ask whether the study accepts your stored sample or needs a new biopsy.

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
650 participants (estimated)
Target follow-up
1 Day
Patient registry
Yes
Biospecimen retention
Samples without dna

Groups and cohorts

  • Patient with COPD

    Procedure: Fiberscopic samples · Procedure: Sputum · Procedure: blood sampling

  • Patient with Asthma

    Procedure: Fiberscopic samples · Procedure: Sputum · Procedure: Nasal brushing · Procedure: blood sampling

  • Healthy volunteer

    Procedure: Fiberscopic samples

Interventions

  • ProcedureFiberscopic samples

    Perform brushing and/or bronchial biopsies and/or BAL and/or aspiration during bronchial fiberscopy and surgical waste during a lobectomy.

  • ProcedureSputum

    Sputum has been collected for biological analysis.

  • ProcedureNasal brushing

    Nasal brushing is a minimally invasive medical procedure used to collect cellular samples from the nasal lining by gently rubbing a small cytology brush against the mucosa.

  • Procedureblood sampling

    Blood sampling is the safe collection of a blood specimen from a vein, finger, or artery to run medical lab tests

06

What researchers measure

Primary outcomes

  1. Describe tobacco consumption

    Number pack in years

    Time frame: At enrollment

  2. Describe tobacco statut

    Described as either non-smokers, former smokers or current smokers

    Time frame: At enrollment

  3. Description of demographic status

    Gender (male or female)

    Time frame: At enrollment

  4. Description of demographic status

    Age as years

    Time frame: At enrollment

  5. Description of demographic status

    Body Mass Index (BMI) (kg/m\^2)

    Time frame: At enrollment

  6. Mesure of lung function parameters

    FEV1: forced expiratory volume in 1 sec

    Time frame: At enrollment

  7. Mesure of lung function parameters

    FVC: forced vital capacity

    Time frame: At enrollment

  8. Mesure of lung function parameters

    FEF25-75: forced expiratory flow between 25 and 75% of the FVC

    Time frame: At enrollment

  9. Mesure of lung function parameters

    TLC: total lung capacity

    Time frame: At enrollment

  10. Mesure of lung function parameters

    RV: residual volume

    Time frame: At enrollment

  11. Describe of disease status

    Described as Healthy, COPD or Asthma

    Time frame: At enrollment

  12. Collection type

    Described as bronchial or lung specimens (frozen of embedded in paraffin), bronchial smooth muscle cells, bronchial epithelial cells, alveolar cells, arterial smooth muscle cells, arterial endothelial cells, fibrocytes, mesenchymal cells, lymphocytes, neutrophils, macrophages, organoïds.

    Time frame: At enrollment

Secondary outcomes

  1. Mesure of blood gas parameter

    PaO2: arterial pressure in oxygen,

    Time frame: At enrollment

  2. Mesure of blood gas parameter

    PaCO2: arterial pressure in carbon dioxide

    Time frame: At enrollment

  3. Mesure of blood gas parameter

    pH

    Time frame: At enrollment

07

Study locations

1 site
  • CHU de Bordeaux
    Pessac, 33604, France
    • Patrick BERGER, PUPH · Contact(+33)05 57 65 65 13
    • Patrick BERGER, MD, PhD · Principal investigator
08

References and documents

Individual participant data

Plan to share: Yes — The data is available from Pr BERGER . An email can be sent to him so that he can contact the data manager and owner, the Bordeaux University Hospital. The data can be made available after contractual agreement.

Supporting information: Study protocol, Statistical analysis plan, Informed consent form, Clinical study report

Time frame: End date

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 21, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07780630
Responsible party
Sponsor
First posted
Aug 21, 2026
Start date
Sep 1, 2026 (estimated)
Primary completion
Dec 31, 2028 (estimated)
Completion
Dec 31, 2028 (estimated)
Last update
Aug 21, 2026

Study contacts

Patrick BERGER, MD, PhD
Contact
patrick.berger@u-bordeaux.fr
+33 5 47 30 27 50

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Aug 2026. You cannot join it, but the record below documents what was studied.

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