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Trial registered on ANZCTR


Registration number
ACTRN12612000458831
Ethics application status
Approved
Date submitted
18/04/2012
Date registered
24/04/2012
Date last updated
6/09/2018
Type of registration
Prospectively registered

Titles & IDs
Public title
Reflux in obstructive sleep apnea
Scientific title
Mechanisms of gastroesophageal reflux in obstructive sleep apnoea
Secondary ID [1] 280356 0
None
Universal Trial Number (UTN)
None
Trial acronym
None
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Obstructive sleep apnoea 286320 0
Gastroesophageal reflux 286321 0
Obesity 286322 0
Condition category
Condition code
Respiratory 286567 286567 0 0
Sleep apnoea
Oral and Gastrointestinal 286594 286594 0 0
Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
The proposed research will investigate the underlying reason for the presence of increased gastroesophageal reflux (GOR) in individuals with obstructive sleep apnoea (OSA) and the effect of OSA treatment on nighttime GOR. In order to examine the role of obesity and arousal from sleep in the presence/severity of nighttime GOR, participants will will undergo in laboratory polysomnography, a 24-hour oesophageal pH-impedance recording and a full body dual energy x-ray absorptiometry scan. In order to examine the effect of CPAP on nighttime GOR in those with and without OSA, participants will undergo 2 consecutive sleep studies and a 48-hour oesophageal pH recording (wireless capsule based measurement, placed during gastroscopy). One of the sleep studies will be with CPAP therapy (set at 10cmH20), and the other night without CPAP. This order will be randomised.

Involvement in the study will span up to 72 hours total.



Intervention code [1] 284721 0
Treatment: Devices
Comparator / control treatment
No control group. However group comparisons will be made - including between obese and non-obese individuals, those with and without OSA those with and without nighttime GOR.
Control group
Uncontrolled

Outcomes
Primary outcome [1] 286994 0
Presence and severity of GOR assessed by pH/impedance testing.
Variables assessed will include: acid contact time, number of acidic and non-acidic reflux events, longest event and number of events > 5 mins.
Timepoint [1] 286994 0
These will be assessed over the 24-hour period as a whole and divided into 'wake time' and 'sleep time' (8 hour sleep study).
Primary outcome [2] 307358 0
Measures of sleep quality and OSA severity as assessed by polysomnography.
Variables include: number of apnoeic/hypopnoeic events, number of arousals and relationship of each arousal to reflux and respiratory events.
Comparisons will be made between groups with and without nighttime GOR and between nights off and on CPAP. The principal analyses for these comparisons will be unpaired or paired t-test.
Timepoint [2] 307358 0
Analyses will be conducted over the 8 hour sleep study.
Secondary outcome [1] 297164 0
Post-hoc analyses will be conducted to determine if the presence and severity of hiatus hernia influences the presence of nighttime GOR or the effect of CPAP on GOR. Presence of hiatus hernia will be detectable during gastroscopy for insertion of the Bravo capsule.
Timepoint [1] 297164 0
Presence of hiatus hernia will be detectable during gastroscopy for insertion of the Bravo capsule.

Eligibility
Key inclusion criteria
18-70 years of age of mixed gender with no significant co-morbidity..

Participants were recruited from patients who had undergone a gastroscopy for investigation of GOR symptoms in the previous 12 months.
Minimum age
18 Years
Maximum age
70 Years
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
Uncontrolled hypertension, ischaemic heart disease, type I diabetes or depression.
Previous oesophageal or gastric surgery
Gastroesophageal disorders such as lupus, coeliac disease or ulcerative colitis.

Study design
Purpose of the study
Treatment
Allocation to intervention
Non-randomised trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Each subject will undergo two conditions - one night of no CPAP and one night of CPAP in a randomised fashion. Therefore there is no need for a procedure for allocating treatment.
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
An online number sequence generator was used with numbers randomly selected from within the range of 0 to 1. Duplicate numbers were allowed. This table was generated on 1/18/2015. http://stattrek.com/statistics/random-number-generator.aspx
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Crossover
Other design features
Phase
Not Applicable
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Date of first participant enrolment
Anticipated
1/06/2012
Actual
1/06/2013
Date of last participant enrolment
Anticipated
Actual
15/08/2017
Date of last data collection
Anticipated
Actual
18/08/2018
Sample size
Target
80
Accrual to date
Final
48
Recruitment in Australia
Recruitment state(s)
WA

Funding & Sponsors
Funding source category [1] 285133 0
Government body
Name [1] 285133 0
National Health and Medical Research Council
Country [1] 285133 0
Australia
Primary sponsor type
University
Name
University of Western Australia
Address
35 Stirling Highway
Crawley WA 6009
Perth, Australia
Country
Australia
Secondary sponsor category [1] 283998 0
Hospital
Name [1] 283998 0
Sir Charles Gairdner Hospital
Address [1] 283998 0
Hospital Avenue, Nedlands WA 6009
Country [1] 283998 0
Australia

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 287149 0
Sir Charles Gairdner Group Human Research Ethics Committee
Ethics committee address [1] 287149 0
Ethics committee country [1] 287149 0
Australia
Date submitted for ethics approval [1] 287149 0
27/03/2012
Approval date [1] 287149 0
17/05/2012
Ethics approval number [1] 287149 0
2012-058

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 34088 0
Prof Peter Eastwood
Address 34088 0
Department of Pulmonary Physiology and Sleep Medicine Internal Mailbox 201 Queen Elizabeth II Medical Centre Hospital Ave Nedlands Western Australia 6009
Country 34088 0
Australia
Phone 34088 0
+61 (08) 6457 1706
Fax 34088 0
Email 34088 0
Peter.Eastwood@health.wa.gov.au
Contact person for public queries
Name 17335 0
Kelly Shepherd
Address 17335 0
Department of Pulmonary Physiology and Sleep Medicine
Internal Mailbox 201
Queen Elizabeth II Medical Centre
Hospital Ave
Nedlands
Western Australia
6009
Country 17335 0
Australia
Phone 17335 0
+61 (08) 6457 3056
Fax 17335 0
+61 (08) 6457 2034
Email 17335 0
Kelly.Shepherd@health.wa.gov.au
Contact person for scientific queries
Name 8263 0
Kelly Shepherd
Address 8263 0
Department of Pulmonary Physiology and Sleep Medicine
Internal Mailbox 201
Queen Elizabeth II Medical Centre
Hospital Ave
Nedlands
Western Australia
6009
Country 8263 0
Australia
Phone 8263 0
+61 (08)9346 3056
Fax 8263 0
+61 (08)9346 2034
Email 8263 0
Kelly.Shepherd@health.wa.gov.au

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.