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Feasibility of Regional Lung Ventilation using X-Ray Velocimetry (XV) in Adult Patients with Chronic Respiratory Conditions.

Not Applicable
Conditions
Chronic Obstructive Pulmonary Disease (COPD)
Asthma
Cystic Fibrosis (CF)
Idiopathic Pulmonary Fibrosis (IPF)
Primary ciliary dyskinesia (PCD)
Respiratory - Chronic obstructive pulmonary disease
Respiratory - Asthma
Respiratory - Other respiratory disorders / diseases
Human Genetics and Inherited Disorders - Cystic fibrosis
Registration Number
ACTRN12623000889651
Lead Sponsor
niversity of New South Wales
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot yet recruiting
Sex
All
Target Recruitment
60
Inclusion Criteria

1. Has a known history of a chronic respiratory condition (such as COPD, asthma, CF, IPF or PCD) that is clinically stable, as defined by no change in medications or hospitalisations, over the preceding four-week period, prior to study recruitment.
2. Male or female adults, 18 years of age and older.
3. Is known to require a chest CT or has a historical chest CT that is representative of the patient’s present lung anatomy (i.e. ideally undertaken within 12-24 months of recruitment to the study).

Exclusion Criteria

1. Currently receiving mechanical ventilation, intensive or other critical care.
2. Pregnant women, confirmed by a positive pregnancy test.
3. Women of child-bearing potential who are unable or unwilling to undergo urine pregnancy test(s) to exclude pregnancy at study visit(s).
4. Contraindication to ionising radiation.
5. Patient weight >150kg (limited by XV scanner’s tolerance).

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To assess the feasibility of the XV scanner for the assessment of lung function in patients with chronic respiratory conditions.<br>Feasibility will be determined comparing XV scan outputs to pulmonary function test measures (spirometric values, MBW, DLCO and lung volumes). [ Primary evaluation will be done at Visit 1A (main study visit). <br><br>]
Secondary Outcome Measures
NameTimeMethod
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