Interstitial Lung Disease Clinical Trial
Official title:
Effective Delivery of Ambulatory Oxygen in Interstitial Lung Disease - a Crossover Trial.
Verified date | June 2014 |
Source | The Alfred |
Contact | n/a |
Is FDA regulated | No |
Health authority | Australia: National Health and Medical Research Council |
Study type | Interventional |
People with interstitial lung disease (ILD) are frequently prescribed ambulatory oxygen, to increase oxygen levels in the blood during daily activities. The best way of delivering this type of oxygen has not been established. The aim of this study is to compare two devices for delivering oxygen in people with interstitial lung disease - the traditional method using portable cylinders and a newer method using a portable concentrator. The investigators hypothesise that oxygen levels during exercise will be significantly higher when using a portable cylinder, but this difference will be small.
Status | Completed |
Enrollment | 10 |
Est. completion date | February 2014 |
Est. primary completion date | February 2014 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - a confident diagnosis of ILD made according to established criteria and - desaturate to less than 90% during a 6-minute walk test Exclusion Criteria: - primary diagnosis of a respiratory condition other than ILD (eg COPD) - currently using continuous oxygen therapy - oxyhaemoglobin saturation (SpO2) is less than 90% on room air - unable to perform a 6-minute walk test or comorbidities that limit walking |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Australia | Alfred Hospital | Melbourne | Victoria |
Lead Sponsor | Collaborator |
---|---|
Anne Holland | The Alfred |
Australia,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Nadir SpO2 | Lowest SpO2 recorded during the 6-min walk test on each device | During 6-min walk test with each oxygen delivery device | No |
Secondary | 6-min walk distance | The distance walked in 6 minutes with each oxygen delivery device will be compared | End 6-min walk test with each oxygen delivery device | No |
Secondary | Borg dyspnoea score | Borg dyspnoea score at the end of the 6-min walk test will be compared between devices | End 6-min walk test with each oxygen delivery device | No |
Secondary | Borg fatigue score | Borg fatigue score at the end of the 6-min walk test will be compared between devices | End 6-min walk test with each oxygen delivery device | No |
Secondary | Partial pressure of oxygen in arterial blood (PaO2) at rest | PaO2 at rest breathing oxygen from each of the two devices will be compared | Prior to 6-min walk test with each oxygen delivery device | No |
Secondary | Proportion of participants who desaturate to less than 80% | Proportion of participants who desaturate to less than 80% with each oxygen delivery device will be compared | During 6-min walk test on each oxygen delivery device | Yes |
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