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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03337854
Other study ID # 2017/44
Secondary ID
Status Not yet recruiting
Phase N/A
First received October 24, 2017
Last updated November 27, 2017
Start date December 20, 2017
Est. completion date December 1, 2018

Study information

Verified date November 2017
Source University Hospital, Bordeaux
Contact François LAURENT, MD, PhD
Phone +335 57 65 63 68
Email francois.laurent@chu-bordeaux.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Chronic obstructive pulmonary disease (COPD) is caused by tobacco consumption. The goal is to characterize on clinical and radiological data, using computed tomography, this illness in order to improve diagnostic and be able to evaluate the prognostic of each patient.


Description:

Chronic obstructive pulmonary disease (COPD) is characterized by emphysematous destruction of pulmonary parenchyma, airway obstruction that participate in chronic temporary obstruction of airways. COPD has multiple clinical presentations that define phenotypes but doesn't take into account those anatomo-pathologic modifications. Moreover, the prognostic interest of those structural alteration is unknown. Until now, only PFT allowed to define the severity of the disease, whereas multiple others tools may be useful, such as, symptoms scores, exacerbation frequencies, denutrition. Those structural alterations are available using computed tomography (CT), that may also have an interest in prognostic or in treatment follow- up.

CT is widely used in clinical practice for COPD patients at basal state and in exacerbations. Quantitative CT is able to combine acquisition of objective and reproductible informations on parenchymal destruction (emphysema), bronchial wall remodeling, and pulmonary vessels alteration. The investigators' team developed software tools to determine quantitative structural modifications of airways, emphysema and small pulmonary vessels1,2.

The team has been able to build a score "Paw score" combining PaO2 with CT parameters of bronchial wall thickness and small pulmonary vessels percentage2. This score allowed to predict the presence of severe pulmonary hypertension in patients with COPD. Pulmonary hypertension is a complication of COPD that increase morbi-mortality.

The hypothesis is that morphological quantitative analysis combined with structural alterations of airways has a prognostic interest.

The main goal is to determine morphological phenotypes of COPD using a cluster analysis combining emphysema, bronchial wall thickness and pulmonary vessels.

The other main goal is to predict evolution of COPD patients based on clinical outcomes (exacerbations frequency, mortality, mMRC, SGQLQ) and lung function testing (decline in FEV-1 TLCO, PaO2).

The team also wants to analyze clinical data of survival, exacerbation and symptoms in following years of the CT of each cluster in historic-prospective way.

The secondary goals are to describe clinical, functional and biological clusters. Analyse of correlations will be studied. Moreover, we will investigate the interest of the "Paw score" as a prognostic marker and as a correlated parameter.

This is a retrospective study. We want to take information from the year before CT, to the year after CT. At the date of the consultation concomitant with CT we want to know all the clinical, functional and biological data of each patient.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 270
Est. completion date December 1, 2018
Est. primary completion date January 1, 2018
Accepts healthy volunteers No
Gender All
Age group 40 Years and older
Eligibility Inclusion Criteria:

- Age = 40 years

- Inhalated toxic exposure:

- Tobacco exposure (present or past, over 10 pack years)

- And/or professional exposure to a toxic

- Obstructive syndrome with a FEV1/FVC = 0.7 after inhalation of a bronchodilatator and measured at stable state (without exacerbation)

- Computed tomography performed without injection contrast during common care

Exclusion Criteria:

- Patients with an exacerbation within 6 weeks before computed tomography

- Artefacts movements on computed tomography incompatible with quantitative analyse

- Broncho-pulmonary cancer (old or present)

- History of pulmonary surgery

- No follow-up for 1 year after scan

- Opposition of the patient to the use of his data (clinical, functional and imaging).

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Centre Hospitalier Universitaire de Bordeaux Bordeaux

Sponsors (2)

Lead Sponsor Collaborator
University Hospital, Bordeaux Transitionnal Research International Laboratory

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Other Number of pack per year of tobacco Number of pack per year of tobacco Day 1
Other Clinical scores Score COPDAssessmentTest "CAT" Scale range: minimum value: 0, maximum value: 40. Only total score is reported. Higher values are considered to be bad outcome. Subscale are not reported, but there are combined by summed to compute the total score. Day 1
Other Clinical scores Score St Georges Scale range: minimum value: 0, maximum value: 3989.4. Only total score is reported. Higher values are considered to be bad outcome. Subscale (symptoms, activities, impact) are not reported, but there are combined by summed to compute the total score. Day 1
Other Clinical scores Score mMRC (Medical Research Council ) Scale range: minimum value: 0, maximum value: 4. Only total score is reported. Higher values are considered to be bad outcome. Day 1
Other Clinical scores Score Global Initiative for Chronic Obstructive Lung Disease (GOLD) Scale range: minimum value: 0, maximum value: 4. Only total score is reported. Higher values are considered to be bad outcome. Day 1
Other Clinical data Six minute walk test (meters, and % predicted) Day 1
Other Pulmonary function test Forced Expiratory Volume - FEV1 (L) Day 1
Other Pulmonary function test Forced Expiratory Volume/ Forced Volume Capacity (FEV1/FVC)(%) Day 1
Other Pulmonary function test value of KCO (Carbon Monoxide Diffusing Capacity (DLCO) divided by Alveolar Volume(VA)) Day 1
Other Pulmonary function test transfer factor of the lung for carbon monoxide (TLCO) Day 1
Other Pulmonary function test total lung capacity (TLC) Day 1
Other Arterial blood gazes pH Day1
Other Arterial blood gazes Partial pressure of oxygen in arterial blood (PaO2) in mmHg Day1
Other Arterial blood gazes Partial pressure of carbon dioxide in arterial blood in mmHg. Day1
Other Arterial blood gazes Hemoglobin (g/dL) Day1
Other Arterial blood gazes carboxyhemoglobin (%) Day1
Other Biology C-reactive protein; cross-reacting protein (mg/l). Day1
Other Biology a1-antitrypsin (mg/l). Day1
Other Clinical parameter weight (kilograms) Day1
Other Clinical parameter Height (meters) Day1
Other Clinical parameter comorbidities Day1
Primary Phenotypes of Chronic obstructive pulmonary disease (COPD) Measure of emphysema Day 1
Primary Phenotypes of Chronic obstructive pulmonary disease (COPD) Measure of proximal bronchial wall thickness Day 1
Primary Phenotypes of Chronic obstructive pulmonary disease (COPD) Measure of dimensions of the pulmonary arteries Day 1
Primary Phenotypes of Chronic obstructive pulmonary disease (COPD) Measure of ratio of main pulmonary artery over aoarta diameter Day 1
Secondary Clinical data of survival Date of death Day 1
Secondary Exacerbations Number of exacerbations Day 1
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