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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/ct2/show/NCT04503564
Registration number
NCT04503564
Ethics application status
Date submitted
9/07/2020
Date registered
7/08/2020
Date last updated
7/03/2023
Titles & IDs
Public title
"FEXIS": (Feasibility of an Extended Wear CSII Set in Participants With T1DM)
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Scientific title
Feasibility of an Investigational Extended Wear Infusion Set for Continuous Subcutaneous Insulin Infusion (CSII) in Type 1 Diabetes Mellitus (T1DM) Participants
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Secondary ID [1]
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ACTRN12620000021976
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Secondary ID [2]
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150-1072-00
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Universal Trial Number (UTN)
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Trial acronym
FEXIS
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Diabetes Mellitus, Type 1
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Type 1 Diabetes
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Type 1 Diabetes Mellitus
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Diabetes Mellitus, Insulin-Dependent, 1
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Condition category
Condition code
Metabolic and Endocrine
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Diabetes
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Treatment: Devices - coil-reinforced soft polymer indwelling cannula
Experimental: Achilles Infusion Set - Coil-reinforced soft polymer indwelling cannula
Treatment: Devices: coil-reinforced soft polymer indwelling cannula
This is a prospective, non-randomized, home-use feasibility study of device performance, usability, tolerability, and safety of the Capillary Biomedical, Inc. (CapBio) Achilles infusion set for continuous subcutaneous insulin infusion (CSII or insulin pump therapy) in up to 20 participants diagnosed with type 1 diabetes mellitus (T1DM).
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Intervention code [1]
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Treatment: Devices
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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Rate of Infusion Set Survival at End of Day 7
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Assessment method [1]
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The composite primary objective of this study is to evaluate feasibility and device performance of the Achilles infusion set over three extended home use wear periods of up to 7 days each during routine therapeutic insulin infusion.
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Timepoint [1]
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7 days during weeks 2 and 3
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Eligibility
Key inclusion criteria
1. Participant is 18 - 70 years of age inclusive
2. Participant is in generally good health, as determined by the investigator
3. Participant is willing and able to individually complete written informed consent and
agrees to comply with all study related testing and examinations
4. Participant must be geographically stable (e.g., expects to be available and capable
of returning for all study specified test and examinations) during the study period
5. Participant has been diagnosed with T1DM for at least 12 months
6. C-peptide less than 0.6 nmol per L at screening
7. Subject can provide a minimum of 14 days of insulin pump data to demonstrate pump use
compliance
8. Participant is willing to perform serum ketone measurements whenever the blood glucose
is determined to be greater than 250 mg per dL (14 mmol per L) using a ketone meter
and strips provided by the sponsor
9. Participant has BMI in the range 20 - 35 kg per square metre inclusive
10. Participant has experience infusing a rapid-acting insulin analog for at least 6
months
11. Participant has been using an insulin pump with commercially available infusion sets
for at least 6 months (this includes Automated Insulin Delivery systems)
12. Participant has previous experience using a continuous glucose monitor (CGM) and is
willing to use a CGM for the duration of the study and perform necessary calibration
fingerstick glucose readings
13. Participant has ability to understand and comply with protocol procedures and to
provide informed consent
14. AST and ALT less than or equal to 120 U per L
15. Creatinine less than 1.8 mg per dL
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Minimum age
18
Years
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Maximum age
70
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
1. Participants whose average total daily insulin dose exceeds 85 units per day (i.e.
typically change insulin reservoirs more often than every 3.5 days on average)
2. Participants who routinely change their commercial insulin infusion sets twice weekly
or less often (wear time greater than 3.5 days)
3. Female participant is pregnant or nursing (Documented negative pregnancy test results
for female participants required unless participant is menopausal without any
spontaneous menstrual cycles for >12 months or key organs have been removed.)
4. Participant has abnormal skin at intended device infusion sites (existing infection,
inflammation, burns, or other extensive scarring)
5. Participant has HbA1C greater than 8.5 percent at screening
6. Participant has documented history in last 6 months of severe hypoglycemia associated
with cognitive dysfunction sufficiently severe to require third party intervention or
a history of impaired awareness of hypoglycemia.
7. Participant has a history of diabetic ketoacidosis in the last 6 months
8. Participant has known cardiovascular disease considered to be clinically relevant by
the investigator
9. Participant has known arrhythmias considered to be clinically relevant by the
investigator
10. Participant has known history of:
1. Cushing's Disease,
2. pancreatic islet cell tumor, or
3. insulinoma
11. Participant has:
1. Lipodystrophy,
2. extensive lipohypertrophy, as assessed by the investigator
12. Participant is undergoing current treatment with:
1. Systemic oral or intravenous corticosteroids,
2. monoamine oxidase (MAO) inhibitors,
3. non-selective beta-blockers,
4. growth hormone,
5. thyroid hormones, unless use has been stable during the past 3 months
13. Subject has significant history of any of the following, that in the opinion of the
investigator would compromise the subject's safety or successful study participation:
1. Alcoholism,
2. drug abuse
14. Significant acute or chronic illness, that in the investigator's opinion, might
interfere with subject safety or integrity of study results
15. Planned operation, MRI or CT which require removal of infusion set or CGM sensor
during wear periods
16. Current participation in another clinical drug or device study
17. AST and ALT greater than 120 U per L
18. Creatinine equal to or greater than 1.8 mg per dL -
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Study design
Purpose of the study
Device Feasibility
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Allocation to intervention
N/A
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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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
Single group
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
13/11/2019
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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
11/11/2020
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Sample size
Target
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Accrual to date
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Final
20
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Recruitment in Australia
Recruitment state(s)
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Recruitment hospital [1]
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St Vincent's Hospital (Melbourne) Ltd - Fitzroy - Melbourne
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Recruitment postcode(s) [1]
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- Melbourne
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Funding & Sponsors
Primary sponsor type
Commercial sector/Industry
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Name
Capillary Biomedical, Inc.
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Address
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Country
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Ethics approval
Ethics application status
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Summary
Brief summary
Over 1 million patients globally currently manage their Type 1 Diabetes mellitus using
continuous subcutaneous insulin infusion with an infusion set that needs to be changed every
3 days. This study will assess the feasibility and device performance of the study device,
the Achilles infusion set over three periods during routine insulin infusion.
This study will include 20 participants and has 3 periods:
Period 1 (up to 7 days): Trial run with study device with saline infusion. Period 2 (up to 7
days): participants will manage their blood glucose solely with their insulin pump and the
Achilles infusion set. Blood glucose will be closely monitored with a continuous glucose
monitoring (CGM) device.
Period 3 (up to 7 days): Participants will return to study center to receive a fresh Achilles
infusion set and continue blood glucose management at home until infusion set failure or 7
days.
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Trial website
https://clinicaltrials.gov/ct2/show/NCT04503564
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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David O'Neal, M.D.
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Address
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St Vincent's Hospital Department of Medicine
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Address
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Country
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Phone
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Fax
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Email
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Contact person for scientific queries
Summary Results
For IPD and results data, please see
https://clinicaltrials.gov/ct2/show/NCT04503564
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