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Trial registered on ANZCTR


Registration number
ACTRN12613000521729
Ethics application status
Approved
Date submitted
20/04/2013
Date registered
10/05/2013
Date last updated
14/05/2013
Type of registration
Prospectively registered

Titles & IDs
Public title
The effect of oxygen on passive inspiratory flow in the apnoeic patient.
Scientific title
The effect of oxygen versus air on passive inspiratory flow rate in women undergoing an elective gynaecological procedure requiring intubation when rendered apnoeic under general anaesthesia.
Secondary ID [1] 282371 0
Nil.
Universal Trial Number (UTN)
U1111-1142-1583
Trial acronym
Apnoeic Flow Study
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Passive inspiratory flow in the apnoeic patient 288953 0
Condition category
Condition code
Anaesthesiology 289285 289285 0 0
Anaesthetics

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
When patient is rendered apnoeic under general anaesthesia, each patient will be with administered oxygen first for ten minutes or less(when SpO2 less than91%), and then with air for ten minutes or less(when SpO2 less than91%).

The flow rate of both oxygen and air will be measured during period of apnoea.

Under normal circumstances the patient will be ventilated when rendered apnoeic. However, we are looking into the physiology of air and oxygen flow in an apnoeic patient.

Oxygen ( 5L/min) and air (5L/min) will be administered over a period of 10 minutes or when patient's pulse oximetry falls below 91%.(which ever occurs first).

Both oxygen and air will be delivered by Anaesthetic machine to patient via the endotracheal tube.

This study occurs at the start of anaesthesia and willll be terminated before the start of surgery.
Intervention code [1] 287003 0
Other interventions
Comparator / control treatment
Air.
Control group
Active

Outcomes
Primary outcome [1] 289396 0
Flow rate of oxygen and air is measured with Eco-medics Vmax 26 flow meter which uses high frequency ultrasonic waves to measure small gas flows in neonates.
Timepoint [1] 289396 0
When flow rate stabilises or at 10 minutes (maximum).
Secondary outcome [1] 302394 0
Nil.
Timepoint [1] 302394 0
Nil.

Eligibility
Key inclusion criteria
Healthy female patients admitted for elective gynaecologycal procedure requiring intubation.

ASA 1-2 patients only.

Body mass index (BMI) between 20 and 35kg per metre square.
Minimum age
18 Years
Maximum age
70 Years
Sex
Females
Can healthy volunteers participate?
No
Key exclusion criteria
Patient refusal.
BMI >35.
Oxygen saturation(peripheral) of less than 95% at room air.
Patients with chronic respiratory disease e.g. asthma.
Patients with features of difficult airway.

Study design
Purpose of the study
Educational / counselling / training
Allocation to intervention
Non-randomised trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Subject will be recruited in the Gynaecology Pre-admission clinic on a voluntary basis. All subjects will receive oxygen first followed by air.
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Single group
Other design features
Phase
Not Applicable
Type of endpoint/s
Safety
Statistical methods / analysis
Univariate data will be expressed as mean(plus minus standard deviation) for parametric data and median(range) for non-parametric data.

Analysis will be done using student's unpaired t-test, Mann-Whitney sum rank test(continuous data), Chi-square test and Fisher Exact (categorical data) as appropriate.

Recruitment
Recruitment status
Not yet recruiting
Date of first participant enrolment
Anticipated
13/05/2013
Actual
Date of last participant enrolment
Anticipated
30/04/2014
Actual
Date of last data collection
Anticipated
Actual
Sample size
Target
18
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
WA
Recruitment hospital [1] 923 0
King Edward Memorial Hospital - Subiaco
Recruitment postcode(s) [1] 6771 0
6008 - Subiaco

Funding & Sponsors
Funding source category [1] 287140 0
Self funded/Unfunded
Name [1] 287140 0
Country [1] 287140 0
Primary sponsor type
Hospital
Name
King Edward Memorial Hospital
Address
374, Bagot Road
Subiaco
WA 6008
Country
Australia
Secondary sponsor category [1] 285909 0
None
Name [1] 285909 0
Address [1] 285909 0
Country [1] 285909 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 289140 0
WNHS Ethics Committee
Ethics committee address [1] 289140 0
Ethics committee country [1] 289140 0
Australia
Date submitted for ethics approval [1] 289140 0
03/08/2012
Approval date [1] 289140 0
04/12/2012
Ethics approval number [1] 289140 0
2051/EW

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

Contacts
Principal investigator
Name 39446 0
Dr Lip Yang Ng
Address 39446 0
Department of Anaesthesia and Pain Medicine
King Edward Memorial Hospital
374, Bagot Road
Subiaco
WA 6008
Country 39446 0
Australia
Phone 39446 0
+61(8) - 9340 2222
Fax 39446 0
+61(8) - 9340 2227
Email 39446 0
[email protected]
Contact person for public queries
Name 39447 0
Lip Yang Ng
Address 39447 0
Department of Anaesthesia and Pain Medicine
King Edward Memorial Hospital
374, Bagot Road
Subiaco
WA 6008
Country 39447 0
Australia
Phone 39447 0
+61(8) - 9340 2222
Fax 39447 0
+61(8) - 9340 2227
Email 39447 0
[email protected]
Contact person for scientific queries
Name 39448 0
Lip Yang Ng
Address 39448 0
Department of Anaesthesia and Pain Medicine
King Edward Memorial Hospital
374, Bagot Road
Subiaco
WA 6008
Country 39448 0
Australia
Phone 39448 0
+61(8) - 9340 2222
Fax 39448 0
+61(8) - 9340 2227
Email 39448 0
[email protected]

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
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