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Impact of a built-in Insulin Calculator Feature on Diabetes Control - Pilot Study

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Abbott Diabetes Care
ClinicalTrials.gov Identifier:
NCT01519466
First received: January 6, 2012
Last updated: November 2, 2012
Last verified: November 2012

January 6, 2012
November 2, 2012
January 2012
October 2012   (final data collection date for primary outcome measure)
Change in time spent in euglycaemia [ Time Frame: Day 1-15 compared with Day 60-74 ] [ Designated as safety issue: No ]
Masked continuous glucose monitoring data will be collected for two weeks at the start of the study and 2 weeks at the end of the study. Analysis will assess the difference between the assessment and baseline phase for the intervention group.
Same as current
Complete list of historical versions of study NCT01519466 on ClinicalTrials.gov Archive Site
  • Change in time spent in euglycaemia [ Time Frame: Day 1-15 compared with Day 60-74 ] [ Designated as safety issue: No ]
    Masked continuous glucose monitoring data will be collected for two weeks at the start of the study and 2 weeks at the end of the study. Analysis will compare the control and intervention groups using analysis of covariance to allow for differences at baseline.
  • Change in HbA1c [ Time Frame: Day 1 compared with Day 74 ] [ Designated as safety issue: No ]
    HbA1c will be tested at baseline (day 1) and then again at end of study (approximately day 74). Analysis will assess the difference between the assessment and baseline results for the intervention group and compare the control and intervention groups.
  • Change in Total Daily Dose (TDD) of insulin [ Time Frame: 5-day diary data collected between Days 1-6 compared with 5-day diary data collected between Days 60-74. ] [ Designated as safety issue: No ]
    5-Day diary data collected during the first 2 weeks of the study will be compared to data collected during the last 2 weeks of the study. Analysis will assess the difference between the assessment and baseline TDD for the intervention group and compare the control and intervention groups.
  • Change in Patient Reported Outcome Measures [ Time Frame: Day 1 compared to Day 60 ] [ Designated as safety issue: No ]
    Diabetes Treatment Satisfaction Questionnaire (DTSQ), Hypoglycaemia Fear Survey (HFS)and Diabetes Distress Scale(DDS)Questionnaires will be completed at Baseline (Day 1) and visit 6 (approximately day 60)and the scores compared. Analysis will assess the difference between the assessment and baseline scores for the intervention group and compare the control and intervention groups.
Same as current
Not Provided
Not Provided
 
Impact of a built-in Insulin Calculator Feature on Diabetes Control - Pilot Study
Impact of a built-in Insulin Calculator Feature on Diabetes Control - Pilot Study

The purpose of this study is to investigate the effect of using FreeStyle InsuLinx (a blood glucose meter with a built-in insulin calculator) on glucose control in people with type 1 diabetes.

Not Provided
Interventional
Not Provided
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Supportive Care
Type 1 Diabetes
  • Device: FreeStyle InsuLinx
    FreeStyle InsuLinx is a blood glucose meter with a built-in insulin calculator feature.
  • Device: FreeStyle Freedom Lite
    FreeStyle Freedom Lite is a blood glucose meter
  • Intervention
    Subjects will use a FreeStyle InsuLinx blood glucose meter during the study
    Intervention: Device: FreeStyle InsuLinx
  • Control
    Subjects will use a FreeStyle Freedom Lite blood glucose meter during the study.
    Intervention: Device: FreeStyle Freedom Lite
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
55
October 2012
October 2012   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Subject with Type 1 diabetes on MDI (3 or more insulin injections per day (U100 insulin)) for at least 1 year and insulin adjusting
  • HbA1c between 7.0% and 9.5% (53 to 80 mmol/mol) inclusive
  • Age 18 and over
  • In the investigator's opinion, thought technically capable of using masked CGM
  • Subject self reporting a minimum of 21 SMBG tests per week prior to study enrolment
  • Willing to perform a minimum of 4 SMBG tests per day during study

Exclusion Criteria:

  • Subject has any concomitant disease or condition that, in the investigator's opinion, may compromise patient safety
  • Subject is participating in another study of a glucose monitoring device / drug that could affect glucose measurements / management
  • Subject is pregnant / planning to become pregnant within the planned study timeline
  • Subject is known to require a dose of more than 50 units of U100 insulin in any one bolus injection
  • Subject is currently on an insulin pump
  • Subject is currently using the FreeStyle InsuLinx
  • Subject is currently using the FreeStyle Freedom Lite
  • Subject is currently using CGM
  • Subject has an allergy to medical grade adhesives
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
Germany,   Netherlands
 
NCT01519466
ADC-PMR-INX-11012
No
Abbott Diabetes Care
Abbott Diabetes Care
Not Provided
Principal Investigator: Prof. Michaela Diamant VU University Medical Centre (VUMC)
Abbott Diabetes Care
November 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP