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Trial registered on ANZCTR
Registration number
ACTRN12605000205639
Ethics application status
Approved
Date submitted
18/08/2005
Date registered
23/08/2005
Date last updated
19/01/2006
Type of registration
Retrospectively registered
Titles & IDs
Public title
Australian Trial of Ventilation in Chronic Airflow Limitation
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Scientific title
Effect of home ventilatory support on clinical outcomes for patients on long term home oxygen therapy.
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Universal Trial Number (UTN)
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Trial acronym
AVCAL
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Chronic airflow limitation
286
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Condition category
Condition code
Respiratory
323
323
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0
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Other respiratory disorders / diseases
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
A comparison of non-invasive nasal ventilation (NIV) during sleep plus long term oxygen therapy (LTOT) versus LTOT alone. The trial takes place over 2 years. In the intervention group, NIV is administered continuously during sleep every night during the trial.
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Intervention code [1]
213
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None
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Comparator / control treatment
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Control group
Active
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Outcomes
Primary outcome [1]
378
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Survival
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Assessment method [1]
378
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Timepoint [1]
378
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At 2 years.
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Secondary outcome [1]
838
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Daytime blood gases
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Assessment method [1]
838
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Timepoint [1]
838
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Measured at 6 monthly intervals
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Secondary outcome [2]
839
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Lung function
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Assessment method [2]
839
0
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Timepoint [2]
839
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Measured at 6 monthly intervals
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Secondary outcome [3]
840
0
Treatment compliance
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Assessment method [3]
840
0
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Timepoint [3]
840
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Measured at 6 monthly intervals
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Secondary outcome [4]
841
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Quality of life
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Assessment method [4]
841
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Timepoint [4]
841
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Measured at 6 monthly intervals
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Eligibility
Key inclusion criteria
Chronic Airflow Limitation (FEV1< 1.5 or < 50% Predicted; FEV1/FVC < 60%, TLC > 92%; FEV1 with bronchodilators < 20%)+Daytime awake PaCO2 >46 mm Hg at least twice in the previous 6 months during periods of clinical stability;+Willing and competent to sign informed consent.+Under 80 years of age+On oxygen therapy for a minimum of three months prior to enrollment.
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Minimum age
Not stated
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Maximum age
80
Years
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Serious coexisting disease (eg. left ventricular failure, malignancy, renal failure, unstable angina) likely to affect survival during the study period+Significant Obstructive Sleep Apnea (defined as Apnoea/hypopoea index >20/h) or Obesity Hypoventilation Syndrome +Significant recent psychological or psychiatric problems likely to significantly impair ability to participate in the study and comply with treatment; +Previous treatment with NIV.
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
No concealment following randomisation
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Sequential envelopes containing random allocations prepared by an independent party
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
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Phase
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
3/01/1998
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
200
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
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Funding & Sponsors
Funding source category [1]
380
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Government body
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Name [1]
380
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NHMRC grant, Application number: 98 1918 (1998-2000)
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Address [1]
380
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Country [1]
380
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Australia
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Funding source category [2]
381
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Government body
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Name [2]
381
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NHMRC grant, Application number: 138404 (2001-2002)
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Address [2]
381
0
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Country [2]
381
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Australia
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Funding source category [3]
382
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Commercial sector/Industry
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Name [3]
382
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Airliquide
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Address [3]
382
0
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Country [3]
382
0
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Primary sponsor type
Individual
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Name
Professor RD McEvoy MD, MBBS
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Address
Director
Adelaide Institute for Sleep Health
Repatriation General Hospital
Daw Park SA
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Country
Australia
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Secondary sponsor category [1]
305
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Individual
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Name [1]
305
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Associate Professor RR Grunstein MBBS, FRACP, MD, PhD, Clinical Associate Professor/Senior Staff Specialist
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Address [1]
305
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Centre for Respiratory Failure and Sleep Disorders
Royal Prince Alfred Hospital
Camperdown NSW
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Country [1]
305
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Australia
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Secondary sponsor category [2]
306
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Individual
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Name [2]
306
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Dr Elizabeth Ellis M.Sc, PhD, Senior Lecturer
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Address [2]
306
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School of Physiotherapy
Faculty of Health Sciences
University of Sydney
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Country [2]
306
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Australia
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Secondary sponsor category [3]
307
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Individual
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Name [3]
307
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Professor RJ Pierce, Head of Respiratory and Sleep Medicine
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Address [3]
307
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Austin and Repatriation Medical Centre
Melbourne VIC
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Country [3]
307
0
Australia
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Secondary sponsor category [4]
308
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Individual
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Name [4]
308
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Dr D Hillman, Director of the Respiratory Physiology Department and Sleep Medicine Service
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Address [4]
308
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Sir Charles Gairdner Hospital
Perth WA
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Country [4]
308
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Australia
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Secondary sponsor category [5]
309
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Individual
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Name [5]
309
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Mr A Esterman MSc, Cstat, DLSHTM, Senior Research Fellow
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Address [5]
309
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Department of General Practice
Flinders University
Adelaide SA
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Country [5]
309
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
1369
0
Repatriation General Hospital
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Ethics committee address [1]
1369
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Daw Park SA
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Ethics committee country [1]
1369
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Australia
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Date submitted for ethics approval [1]
1369
0
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Approval date [1]
1369
0
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Ethics approval number [1]
1369
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Ethics committee name [2]
1370
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Royal Prince Alfred Hospital
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Ethics committee address [2]
1370
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Camperdown NSW
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Ethics committee country [2]
1370
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Australia
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Date submitted for ethics approval [2]
1370
0
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Approval date [2]
1370
0
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Ethics approval number [2]
1370
0
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Ethics committee name [3]
1371
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Austin and Repatriation Hospital
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Ethics committee address [3]
1371
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Heidelberg Vic
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Ethics committee country [3]
1371
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Australia
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Date submitted for ethics approval [3]
1371
0
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Approval date [3]
1371
0
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Ethics approval number [3]
1371
0
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Ethics committee name [4]
1372
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Sir Charles Gairdner Hospital
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Ethics committee address [4]
1372
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Perth WA
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Ethics committee country [4]
1372
0
Australia
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Date submitted for ethics approval [4]
1372
0
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Approval date [4]
1372
0
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Ethics approval number [4]
1372
0
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Ethics committee name [5]
1373
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The Royal Adelaide Hospital
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Ethics committee address [5]
1373
0
Adelaide SA
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Ethics committee country [5]
1373
0
Australia
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Date submitted for ethics approval [5]
1373
0
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Approval date [5]
1373
0
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Ethics approval number [5]
1373
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Ethics committee name [6]
1374
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Queen Elizabeth Hospital
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Ethics committee address [6]
1374
0
Adelaide SA
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Ethics committee country [6]
1374
0
Australia
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Date submitted for ethics approval [6]
1374
0
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Approval date [6]
1374
0
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Ethics approval number [6]
1374
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Ethics committee name [7]
1375
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The Alfred and Hospital
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Ethics committee address [7]
1375
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Melbourne VIC
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Ethics committee country [7]
1375
0
Australia
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Date submitted for ethics approval [7]
1375
0
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Approval date [7]
1375
0
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Ethics approval number [7]
1375
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Ethics committee name [8]
1376
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Flinders University
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Ethics committee address [8]
1376
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Bedford Park SA
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Ethics committee country [8]
1376
0
Australia
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Date submitted for ethics approval [8]
1376
0
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Approval date [8]
1376
0
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Ethics approval number [8]
1376
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Summary
Brief summary
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
35261
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Address
35261
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Country
35261
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Phone
35261
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Fax
35261
0
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Email
35261
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Contact person for public queries
Name
9402
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Professor R Doug McEvoy
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Address
9402
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Adelaide Institute for Sleep Health
Repatriation General Hospital
Daw Park SA 5041
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Country
9402
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Australia
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Phone
9402
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+61 8 82751187
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Fax
9402
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+61 8 82776890
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Email
9402
0
[email protected]
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Contact person for scientific queries
Name
330
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Professor R Doug McEvoy
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Address
330
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Adelaide Institute for Sleep Health
Repatriation General Hospital
Daw Park SA 5041
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Country
330
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Australia
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Phone
330
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+61 8 82751187
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Fax
330
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+61 8 82751187
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Email
330
0
[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
Download to PDF