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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01906931
Other study ID # 187_13
Secondary ID
Status Completed
Phase Phase 2
First received July 16, 2013
Last updated June 23, 2014
Start date August 2013
Est. completion date February 2014

Study information

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

Clinical Trial Summary

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.


Description:

Exercise-induced hypoxaemia (EIA) is very common in individuals with ILD, due to progressive lung fibrosis which results in impaired gas exchange. It is common for people with EIA to be prescribed ambulatory oxygen, in order to normalize oxyhaemoglobin saturation, improve oxygen delivery to the tissues and relieve breathlessness during daily activities.

Ambulatory oxygen is traditionally delivered via a refillable portable oxygen cylinder containing compressed gaseous oxygen. More recently, portable oxygen concentrators (POCs) have emerged as a solution to the problem of finite cylinder life and to improve portability. Because a concentrator is constantly extracting oxygen from air, oxygen supply can continue as long as the battery is charged. This is typically around eight hours, but POCs can be recharged from an AC or DC power source. Portable oxygen concentrators usually weigh around 3.5kg, which is significantly lighter than oxygen cylinders, and are much easier to maneuver. However, there are some theoretical disadvantages to POCs. Like all concentrators, they do not deliver 100% oxygen. Concentrations typically range from 85-95%, depending on the flow rate. Differences in pulse timing and peak pulse flow between POCs may affect the fraction of inspired oxygen (FiO2) that is delivered. However, the clinical implications of these differences have not been documented.

The aim of this study is to compare the effects of ambulatory oxygen delivered during exercise using the EverGo POC to ambulatory oxygen delivered with a standard portable cylinder in individuals with ILD. We hypothesise that oxyhaemoglobin saturation during exercise will be significantly higher when using a portable cylinder, but this difference will not be clinically important.


Recruitment information / eligibility

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

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Intervention

Device:
Portable oxygen concentrator
Respironics EverGo portable oxygen concentrator on setting 6
Portable oxygen cylinder
Portable oxygen cylinder at flow rate 5 Litres/min

Locations

Country Name City State
Australia Alfred Hospital Melbourne Victoria

Sponsors (2)

Lead Sponsor Collaborator
Anne Holland The Alfred

Country where clinical trial is conducted

Australia, 

Outcome

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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