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Evidence-based Analysis of Low-dose CT in Management of COPD

Primary Purpose

Chronic Obstructive Pulmonary Disease

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Low-Dose Computed Tomography
Sponsored by
Azienda Ospedaliero-Universitaria di Parma
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Chronic Obstructive Pulmonary Disease focused on measuring Chronic Obstructive Pulmonary Disease, Diagnostic Imaging, Disease Management, Clinical Decision Support Systems, Cost-Utility Analysis

Eligibility Criteria

40 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • COPD diagnosis according to ATS/ERS criteria (post-bronchodilator FEV1 to FVC ratio < 0.7);
  • clinical stability, namely no acute exacerbation in the previous 4 weeks;
  • clinical indication for low-dose computed tomography (LDCT) to investigate bronchiectasis, interstitial lung disease, or pulmonary hypertension.

Exclusion Criteria:

  • pregnancy;
  • patients with congenital or acquired immune deficit;
  • patients with lung transplantation;
  • patients under oxygen therapy;
  • patients with diagnosis of asthma or other clinically relevant pulmonary disease other than COPD.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    MulticenterRecruitment

    Arm Description

    COPD phenotypization by Low-Dose Computed Tomography

    Outcomes

    Primary Outcome Measures

    Impact of diagnostic imaging in assessing COPD by qualitative and quantitative evaluation (questionnaire)
    To quantify the refinement of the diagnosis of COPD patients when LDCT data are added to standard evaluation, namely, conventional clinical-functional assessment and chest radiography.
    Clinical management of COPD in relation to therapy adjustment (questionnaire)
    To describe the change in management of COPD patients when LDCT data are added to standard evaluation, namely, conventional clinical-functional assessment and chest radiography.

    Secondary Outcome Measures

    Intra-observer agreement before and after disclosure of LDCT features (questionnaire)
    To assess the intra-observer agreement of pulmonologists before and after assimilation of LDCT data.
    Inter-observer agreement (questionnaire)
    To assess changes in inter-observer agreement between pulmonologist before and after assimilation of LDCT data.
    Additional costs derived from change in management of COPD after disclosure of LDCT features (comparison of costs)
    To evaluate additional costs for the regional health care system deemed by assimilation of LDCT data.

    Full Information

    First Posted
    November 4, 2015
    Last Updated
    November 5, 2015
    Sponsor
    Azienda Ospedaliero-Universitaria di Parma
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02599883
    Brief Title
    Evidence-based Analysis of Low-dose CT in Management of COPD
    Official Title
    Impact of Low-dose Computed Tomography on the Management of Chronic Obstructive Pulmonary Disease Patients: an Evidence-based Study
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    November 2015
    Overall Recruitment Status
    Completed
    Study Start Date
    September 2012 (undefined)
    Primary Completion Date
    September 2015 (Actual)
    Study Completion Date
    September 2015 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Azienda Ospedaliero-Universitaria di Parma

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Background: Chronic obstructive pulmonary disease (COPD) is the fourth leading cause of chronic morbidity and mortality worldwide. There is debate about diagnosis and management of COPD because it was described as complex syndrome accounting for various pulmonary and extrapulmonary abnormalities. As a result, there is consensus that both clinical evaluation and pulmonary function tests (PFTs) data by themselves do not adequately describe the complexity of the disease. The chest radiograph is the sole imaging examination recommended for the routine evaluation of these patients by the physicians guidelines (GOLD guidelines),which, however, are also debating on the utility of computed tomography (CT) in this setting. Indeed, a number of studies reported a dramatic increasing use of CT of the chest for COPD assessment, in both clinical and research settings. COPD assessment by CT seems to improve the accuracy and completeness of the clinical evaluation of these patients. Nevertheless, the clinical utility of CT has yet to be proved by prospective studies or defined by guidelines. Objectives: To evaluate the change in the diagnosis and management of COPD when multiple CT-derived information is added to pre-test evaluation. Methods: Four pulmonologists with various expertise in the field will review clinical data, PFTs results, and chest radiographs of 200 consecutive COPD patients diagnosed according to current guidelines. Therefore, after two months from the first evaluation, the pulmonologists will review the clinical and PFTs records with comprehensive information about low-dose CT (LDCT) previously performed in a week from the chest radiograph. Information about LDCT findings will include qualitative assessment by an experienced chest radiologist and quantitative analysis by means of an innovative 3D imaging dedicated software. Phenotype assessment and patient care decisions (e.g. therapeutic and follow-up strategies, need of additional tests etc.) will be recorded before and after assimilation of LDCT data. Expected results: This evidence-based prospective study will test the impact of chest LDCT on management of COPD patient. In addition, the level of agreement between pulmonologists in terms of diagnosis and therapeutic strategies will be assessed. Furthermore, the study will evaluate the need for additional tests referable to LDCT information and their impact on the health care system (e.g. in terms of additional costs).

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Chronic Obstructive Pulmonary Disease
    Keywords
    Chronic Obstructive Pulmonary Disease, Diagnostic Imaging, Disease Management, Clinical Decision Support Systems, Cost-Utility Analysis

    7. Study Design

    Primary Purpose
    Diagnostic
    Study Phase
    Not Applicable
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    195 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    MulticenterRecruitment
    Arm Type
    Experimental
    Arm Description
    COPD phenotypization by Low-Dose Computed Tomography
    Intervention Type
    Radiation
    Intervention Name(s)
    Low-Dose Computed Tomography
    Intervention Description
    Low-Dose Computed Tomography will be administered to COPD patients as part of COPD phenotypization.
    Primary Outcome Measure Information:
    Title
    Impact of diagnostic imaging in assessing COPD by qualitative and quantitative evaluation (questionnaire)
    Description
    To quantify the refinement of the diagnosis of COPD patients when LDCT data are added to standard evaluation, namely, conventional clinical-functional assessment and chest radiography.
    Time Frame
    Up to 3 years
    Title
    Clinical management of COPD in relation to therapy adjustment (questionnaire)
    Description
    To describe the change in management of COPD patients when LDCT data are added to standard evaluation, namely, conventional clinical-functional assessment and chest radiography.
    Time Frame
    Up to 3 years
    Secondary Outcome Measure Information:
    Title
    Intra-observer agreement before and after disclosure of LDCT features (questionnaire)
    Description
    To assess the intra-observer agreement of pulmonologists before and after assimilation of LDCT data.
    Time Frame
    Up to 3 years
    Title
    Inter-observer agreement (questionnaire)
    Description
    To assess changes in inter-observer agreement between pulmonologist before and after assimilation of LDCT data.
    Time Frame
    Up to 3 years
    Title
    Additional costs derived from change in management of COPD after disclosure of LDCT features (comparison of costs)
    Description
    To evaluate additional costs for the regional health care system deemed by assimilation of LDCT data.
    Time Frame
    Up to 3 years

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    40 Years
    Maximum Age & Unit of Time
    90 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: COPD diagnosis according to ATS/ERS criteria (post-bronchodilator FEV1 to FVC ratio < 0.7); clinical stability, namely no acute exacerbation in the previous 4 weeks; clinical indication for low-dose computed tomography (LDCT) to investigate bronchiectasis, interstitial lung disease, or pulmonary hypertension. Exclusion Criteria: pregnancy; patients with congenital or acquired immune deficit; patients with lung transplantation; patients under oxygen therapy; patients with diagnosis of asthma or other clinically relevant pulmonary disease other than COPD.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Nicola Sverzellati, MD, PhD
    Organizational Affiliation
    Università di Parma
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Learn more about this trial

    Evidence-based Analysis of Low-dose CT in Management of COPD

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