NCT02599883

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).

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
195

participants targeted

Target at P75+ for not_applicable chronic-obstructive-pulmonary-disease

Timeline
Completed

Started Sep 2012

Longer than P75 for not_applicable chronic-obstructive-pulmonary-disease

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

September 1, 2012

Completed
3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2015

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2015

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

November 4, 2015

Completed
5 days until next milestone

First Posted

Study publicly available on registry

November 9, 2015

Completed
Last Updated

November 9, 2015

Status Verified

November 1, 2015

Enrollment Period

3 years

First QC Date

November 4, 2015

Last Update Submit

November 5, 2015

Conditions

Keywords

Chronic Obstructive Pulmonary DiseaseDiagnostic ImagingDisease ManagementClinical Decision Support SystemsCost-Utility Analysis

Outcome Measures

Primary Outcomes (2)

  • 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.

    Up to 3 years

  • 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.

    Up to 3 years

Secondary Outcomes (3)

  • Intra-observer agreement before and after disclosure of LDCT features (questionnaire)

    Up to 3 years

  • Inter-observer agreement (questionnaire)

    Up to 3 years

  • Additional costs derived from change in management of COPD after disclosure of LDCT features (comparison of costs)

    Up to 3 years

Study Arms (1)

MulticenterRecruitment

EXPERIMENTAL

COPD phenotypization by Low-Dose Computed Tomography

Radiation: Low-Dose Computed Tomography

Interventions

Low-Dose Computed Tomography will be administered to COPD patients as part of COPD phenotypization.

MulticenterRecruitment

Eligibility Criteria

Age40 Years - 90 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Pulmonary Disease, Chronic Obstructive

Condition Hierarchy (Ancestors)

Lung Diseases, ObstructiveLung DiseasesRespiratory Tract DiseasesChronic DiseaseDisease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • Nicola Sverzellati, MD, PhD

    Università di Parma

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
DIAGNOSTIC
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor, MD, PhD

Study Record Dates

First Submitted

November 4, 2015

First Posted

November 9, 2015

Study Start

September 1, 2012

Primary Completion

September 1, 2015

Study Completion

September 1, 2015

Last Updated

November 9, 2015

Record last verified: 2015-11