Trial Review

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Trial registered on ANZCTR


Registration number
ACTRN12620000401954
Ethics application status
Approved
Date submitted
26/02/2020
Date registered
25/03/2020
Date last updated
25/03/2020
Date data sharing statement initially provided
25/03/2020
Type of registration
Prospectively registered

Titles & IDs
Public title
Effect of kiwifruit consumption on gastric emptying
Scientific title
Effect of kiwifruit consumption on gastric emptying - A randomised, repeated measures, human intervention study
Secondary ID [1] 300582 0
Nil known
Universal Trial Number (UTN)
U1111-1247-3467
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Diabetes 316319 0
Metabolic disorder 316320 0
Condition category
Condition code
Metabolic and Endocrine 314587 314587 0 0
Other metabolic disorders
Metabolic and Endocrine 314948 314948 0 0
Diabetes

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
A randomised repeated measures design will be used in which each subject receives all diets in a random order.
The test foods will be as follows:
1. Weet-Bix only (40 g available carbohydrate)
2. Weet-Bix (20g available carbohydrate) plus kiwifruit (20g available carbohydrate)

13C-labelled sodium acetate (100 mg) will be added to the test meal just before consumption (details on the safety of 13C-labelled sodium acetate is stated below).

An additional 200 ml of water will be consumed with all diets.

On each test day the volunteers will be seated and asked to remain so for the duration of the test. They may continue work, if practical to do so, at the testing location. Once each subject is relaxed and comfortable (approximately 15-20 minutes after arrival), a baseline blood sugar measurement will be taken in duplicate for that day. Each subject will then be given a test food and instructed to consume the whole amount within a ten-minute period.
The duration of each testing session be 3 hours and 45 minutes.
The duration of the washout between each testing session will be 48 hours
Intervention code [1] 316893 0
Prevention
Intervention code [2] 316894 0
Lifestyle
Comparator / control treatment
Control - Weetbix

All results will be compared with the results obtained for weetbix
Control group
Active

Outcomes
Primary outcome [1] 322919 0
Gastric emptying as assessed by exhaled breath analysis
Timepoint [1] 322919 0
Breath samples will be collected by blowing gently into a 10ml Exetainer with a drinking straw and replacing the cap just before the end of exhalation. Breath samples will be collected at baseline (time = zero minutes) and every 15 min postprandially until 3 hours. Breath samples will be analysed using isotope ratio mass spectrometry.
Primary outcome [2] 322920 0
Blood glucose as assessed by finger-prick blood test
Timepoint [2] 322920 0
Blood glucose testing will be timed from the start of food consumption by finger prick sampling of capillary blood at 15 min intervals in the first hour and then at 30 min intervals until 180 min has elapsed. Samples will be collected at 0 (baseline x 2), 15, 30, 45, 60, 90, 120, 150 and 180 minutes. The blood glucose will be measured immediately using a HemoCue® blood glucose meter
Secondary outcome [1] 380242 0
Measure changes in insulin
Timepoint [1] 380242 0
Blood sampling will be timed from the start of food consumption by finger prick sampling of capillary blood at 15 min intervals in the first hour and then at 30 min intervals until 180 min has elapsed. Samples will be collected at 0 (baseline x 2), 15, 30, 45, 60, 90, 120, 150 and 180 minutes.
Capillary blood sample will be drawn into a Z gel serum Microvette® microtube designed for capillary blood collection, centrifuged and stored at -80°C for later analysis
Secondary outcome [2] 381339 0
Measure changes in increatin hormones (gastric inhibitory peptide (GIP) and glucagon-like peptide-1 (GLP-1).
Timepoint [2] 381339 0
Blood sampling will be timed from the start of food consumption by finger prick sampling of capillary blood at 15 min intervals in the first hour and then at 30 min intervals until 180 min has elapsed. Samples will be collected at 0 (baseline x 2), 15, 30, 45, 60, 90, 120, 150 and 180 minutes.
Capillary blood sample will be drawn into a Z gel serum Microvette® microtube designed for capillary blood collection, centrifuged and stored at -80°C for later analysis
Secondary outcome [3] 381340 0
Satiety will also be measured using 'Visual Analogue Scale'
Timepoint [3] 381340 0
Time: 0, 15, 30, 45, 60, 90, 120, 150 and 180 minutes.

Eligibility
Key inclusion criteria
Inclusion criteria:
• Age: Aged between 18 and 40.
• Sex: Male or female.
• Glucose tolerance: No history of diabetes or evidence of glucose intolerance in a preliminary screening test.
• BMI: Volunteers have a body mass index between 18.5 and 24.99 kg/m2
• Health: Healthy as gauged by self-assessment and result on the General Health Questionnaire.
• Agreement: Subject having given written informed consent to comply with the conditions of the trial.
Minimum age
18 Years
Maximum age
40 Years
Sex
Both males and females
Can healthy volunteers participate?
Yes
Key exclusion criteria
Exclusion criteria:
• Glucose intolerance: Any history of diabetes or evidence of glucose intolerance in a preliminary test (greater than or equal to 6.0mmol/l fasting glucose, International Diabetes Federation recommendation) and HbA1c greater than 40 mmol/mol
• Non-fasting: Having consumed anything apart from water in the twelve hours prior to the test.
• Allergic or intolerant kiwifruit or wheat
• Pregnant or breastfeeding.
• Long term chronic illnesses requiring treatment, such as cancer and cardiovascular disease.
• Gut conditions or drugs effecting gut transit time, such as irritable bowel syndrome, peptic ulcers and laxatives.

Study design
Purpose of the study
Prevention
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Each participant will be assigned an identification number, including those who fail the screening procedure by central randomization by computer.

Participants who pass the screening procedure will be allocated numbers after the recruitment process is finished. Therefore, the recruiter was unaware of the treatment order for each individual at time of recruiting. Each participant receives all treatments in random order rather than being allocated to one group. Randomization of the samples and treatments will be completed by a statistician at Plant & Food Research using a computer.
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
The order of the diets and treatments for each subject (n=10) will be determined by computer randomisation of numbers
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Crossover
Other design features
Phase
Not Applicable
Type of endpoint/s
Efficacy
Statistical methods / analysis
Groups will be compared in terms of gastric emptying rate and response amplitude, time 0 baseline and incremental area under the curve for blood glucose response, insulin and the incretin hormones by comparison of treatments. A registered statistician at Plant and Food Research will conduct the statistical analysis.

Recruitment
Recruitment status
Not yet recruiting
Date of first participant enrolment
Anticipated
1/04/2020
Actual
Date of last participant enrolment
Anticipated
30/04/2020
Actual
Date of last data collection
Anticipated
19/06/2020
Actual
Sample size
Target
10
Accrual to date
Final
Recruitment outside Australia
Country [1] 22384 0
New Zealand
State/province [1] 22384 0
Manawatu

Funding & Sponsors
Funding source category [1] 305004 0
Government body
Name [1] 305004 0
The New Zealand Institute for Plant and Food Research
Country [1] 305004 0
New Zealand
Primary sponsor type
Government body
Name
Crown Research Organisation
Address
New Zealand Institute for Plant and Food Research,\
Batchelar Road,
Fitzherbert Science Centre,
Palmerston North 4442
Country
New Zealand
Secondary sponsor category [1] 305360 0
None
Name [1] 305360 0
None
Address [1] 305360 0
None
Country [1] 305360 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 305400 0
Northern B Health and Disability Ethics Committee
Ethics committee address [1] 305400 0
Ethics committee country [1] 305400 0
New Zealand
Date submitted for ethics approval [1] 305400 0
05/02/2020
Approval date [1] 305400 0
09/03/2020
Ethics approval number [1] 305400 0
20/CEN/28

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

Contacts
Principal investigator
Name 100250 0
Dr John Monro
Address 100250 0
Plant and Food Research
Food Industry Science Centre
Private Bag 11600
Palmerston North 4442
Country 100250 0
New Zealand
Phone 100250 0
+64 63556137
Fax 100250 0
Email 100250 0
[email protected]
Contact person for public queries
Name 100251 0
John Monro
Address 100251 0
Plant and Food Research
Food Industry Science Centre
Private Bag 11600
Palmerston North 4442
Country 100251 0
New Zealand
Phone 100251 0
+64 63556137
Fax 100251 0
Email 100251 0
[email protected]
Contact person for scientific queries
Name 100252 0
John Monro
Address 100252 0
Plant and Food Research
Food Industry Science Centre
Private Bag 11600
Palmerston North 4442
Country 100252 0
New Zealand
Phone 100252 0
+64 63556137
Fax 100252 0
Email 100252 0
[email protected]

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
No/undecided IPD sharing reason/comment


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.