Trial Review

The ANZCTR website will be unavailable from 1pm until 3pm (AEDT) on Wednesday the 30th of October for website maintenance. Please be sure to log out of the system in order to avoid any loss of data.

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been endorsed by the ANZCTR. Before participating in a study, talk to your health care provider and refer to this information for consumers
Trial registered on ANZCTR


Registration number
ACTRN12620000535976
Ethics application status
Approved
Date submitted
9/03/2020
Date registered
1/05/2020
Date last updated
1/05/2020
Date data sharing statement initially provided
1/05/2020
Type of registration
Prospectively registered

Titles & IDs
Public title
Atmo Gas capsule localisation study in healthy volunteers
Scientific title
Validation of Atmo Gas capsule localising technique via intestinal ultrasound in healthy volunteers
Secondary ID [1] 299849 0
AH-ALS02
Universal Trial Number (UTN)
U1111-1243-8772
Trial acronym
N/A
Linked study record
This record is a follow-up study for ACTRN12619001219178

Health condition
Health condition(s) or problem(s) studied:
Gastrointestinal dysmotility
 316880 0
Condition category
Condition code
Oral and Gastrointestinal 313550 313550 0 0
Normal oral and gastrointestinal development and function

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
The study will involve ingestion of a wireless, gas-sensing (Atmo) capsule with simultaneous gastrointestinal ultrasound (GIUS) imaging to validate the localisation of the Atmo capsule. This study will occur once.

Following an overnight fast, the subjects will arrive at the Department of Gastroenterology, Alfred Hospital for the study. A baseline gastrointestinal ultrasound (GIUS) will be performed by an experienced GIUS-trained gastroenterologist to assess the participant's basic abdominal anatomy (the participant will be consenting and fully awake and be able to see the scan in real-time). The images from this scan are not recorded.

Following ingestion of the Atmo capsule, dynamic scanning using GIUS will commence following the transit of the capsule through the stomach and small intestine. Ultrasound images of the capsule passing through the pylorus (stomach) and ileocaecal junction will be taken. Images of these landmarks will record time and proof of capsule transit. Data will be collected in a coded manner. Ultrasound imaging will cease once arrival of the capsule in the large intestine has been confirmed.

Additionally, once the ultrasound imaging has been completed, participants will be allowed to leave the facility. Instructions on confirming passage of capsule during a bowel movement will be provided. It is anticipated that the Atmo capsule will take approximately 24-48 h to pass through the gastorintestinal system. Participants will also be instructed to keep the Atmo receiver close to their body (within 1.5 m) at all times.
Intervention code [1] 316106 0
Treatment: Devices
Comparator / control treatment
Gastrointestinal ultrasound (GIUS)

Gastrointestinal ultrasound is an attractive technique that is easily accessible and is not associated with radiation risk to participants. This method can recognise and distinguish anatomical structures according wall characteristics, size, contents and motility patterns. Thus, stomach, small bowel and colon have different appearances. The gas capsule is readily recognised sonographically. Visualisation of the gas capsule within the gastrointestinal tract has previously been performed in one healthy volunteer with good success. Additionally, with the improved image resolution of latest generation of GIUS machines and the clear visibility of the capsule sonographically. GIUS is able to accurately identify the ileo-caecal junction and, therefore, distinguish small and large intestine.

As outlined above, dynamic ultrasound scanning will be performed immediately from ingestion of Atmo capsule following the transit of the gas capsule throughout the gastrointestinal tract for the next 6 - 8 h. Continuous scanning will occur if gastric emptying or passage to the ileocaecal junction is anticipated.
Control group
Uncontrolled

Outcomes
Primary outcome [1] 323181 0
(a) confirmation of gastric emptying landmark using a composite of
(i) the time at which the first gradient inflection for the motility marker was recorded in the stomach (verified visually via graphs generated by the Atmo data receiver) AND
(ii) the times that direct visualisation of the capsule disappeared from the stomach/entered the duodenum on sonographic imaging.
Timepoint [1] 323181 0
Estimated within 4 h after ingestion of the Atmo capsule
Primary outcome [2] 323182 0
(b) confirmation of ileal-caecal junction using a composite of
(i) the time at which a second gradient inflection for the O2-equivalent motility marker was recorded after gastric emptying and no further temperature drop associated with water ingestion have occurred
AND
(b) the time via sonographic imaging that direct visualisation of the capsule entered the caecum.
Timepoint [2] 323182 0
Estimated within 6-8 h post-Atmo capsule ingestion
Secondary outcome [1] 381096 0
Gastric emptying time assessed by the Atmo capsule, defined as the duration between capsule ingestion and gastric emptying landmark and verified by sonographic images as the appearance of the capsule in the duodenum
Timepoint [1] 381096 0
Within 4 h post capsule ingestion
Secondary outcome [2] 381667 0
Whole gut transit time assessed by the Atmo capsule, defined as the duration between capsule ingestion and expulsion.
Timepoint [2] 381667 0
Within 24-48 h post-capsule ingestion
Secondary outcome [3] 381672 0
Small bowel transit times defined by duration between gastric emptying and proposed ileal-caecal junction as assessed using data from the Atmo capsule and verified by sonographic images.
Timepoint [3] 381672 0
Within 6-8 h
Secondary outcome [4] 381673 0
large bowel transit time defined as duration between ileal-caecal junction and passage of capsule as denoted by temperature drop or loss of signal coinciding with a bowel movement
Timepoint [4] 381673 0
Within 24-36 h

Eligibility
Key inclusion criteria
Healthy controls without known gastrointestinal disease/disorder
Minimum age
18 Years
Maximum age
55 Years
Sex
Both males and females
Can healthy volunteers participate?
Yes
Key exclusion criteria
history of gastrointestinal, endocrine or neurological disorders known to influence gastrointestinal motility, dysphagia, presence of suspected strictures, radiation enteritis or gastric bezoar; pregnancy; individuals with a body mass index >30 kg/m2, those with previous abdominal surgery (except appendicectomy) or implantable devices such as a pacemaker; antibiotic, prebiotic or probiotic use in the last 4 weeks; intake of proton pump inhibitors, H2 receptor antagonists, antacids in the last 7 days or prokinetics in the last 2 days; those who are currently receiving diathermy or have planned MRI or diathermy in the next 2 months.

Study design
Purpose of the study
Diagnosis
Allocation to intervention
Non-randomised trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
None
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
None
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
Bio-equivalence
Statistical methods / analysis
Descriptive data will be used to report the outcomes of the study. Comparison will be made between (a) the times of exit from the stomach and the first O2-equivalent gradient inflection; and (b) the times of the passage of the capsule into the caecum and the occurrence of anaerobic conditions. Equivalence will be defined as an agreement of less than or equal to 25% between the two devices (or less than or equal to 30% as previously defined by Rao et al. 2009). A second approach to demonstrating equivalence will also be explored via linear regression and by assessing degrees of agreement between the paired time points using the Bland-Altman plots. Agreement is considered strong if 95% values lie within ±2 SD of mean differences. The results, conduct and reporting of the study will conform with the STARD 2015 guidelines (http://www.equator-network.org/reporting-guidelines/stard/).

Recruitment
Recruitment status
Not yet recruiting
Date of first participant enrolment
Anticipated
1/06/2020
Actual
Date of last participant enrolment
Anticipated
1/11/2020
Actual
Date of last data collection
Anticipated
1/12/2020
Actual
Sample size
Target
15
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
VIC
Recruitment hospital [1] 16099 0
The Alfred - Melbourne
Recruitment postcode(s) [1] 29613 0
3004 - Melbourne

Funding & Sponsors
Funding source category [1] 304306 0
Commercial sector/Industry
Name [1] 304306 0
Atmo Biosciences
Country [1] 304306 0
Australia
Primary sponsor type
University
Name
Monash University
Address
Level 6 The Alfred Centre
99 Commercial Rd
Melbourne VIC 3004
Country
Australia
Secondary sponsor category [1] 304551 0
None
Name [1] 304551 0
Address [1] 304551 0
Country [1] 304551 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 304759 0
Monash University Human Research Ethics Committee
Ethics committee address [1] 304759 0
Ethics committee country [1] 304759 0
Australia
Date submitted for ethics approval [1] 304759 0
11/11/2019
Approval date [1] 304759 0
11/12/2019
Ethics approval number [1] 304759 0
22438

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

Contacts
Principal investigator
Name 98114 0
Prof Peter Gibson
Address 98114 0
Level 6 The Alfred Centre
99 Commercial Rd
Melbourne VIC 3004
Country 98114 0
Australia
Phone 98114 0
+61399030640
Fax 98114 0
Email 98114 0
[email protected]
Contact person for public queries
Name 98115 0
CK Yao
Address 98115 0
Level 6 The Alfred Centre
99 Commercial Rd
Melbourne VIC 3004
Country 98115 0
Australia
Phone 98115 0
+61399030266
Fax 98115 0
Email 98115 0
[email protected]
Contact person for scientific queries
Name 98116 0
CK Yao
Address 98116 0
Level 6 The Alfred Centre
99 Commercial Rd
Melbourne VIC 3004
Country 98116 0
Australia
Phone 98116 0
+61399030266
Fax 98116 0
Email 98116 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
As this is a industry-funded project, data will by only be available via manuscript for publication in an international peer reviewed journal.


What supporting documents are/will be available?

Doc. No.TypeCitationLinkEmailOther DetailsAttachment
7296Ethical approval    378764-(Uploaded-09-03-2020-20-52-54)-Study-related document.pdf



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.