Last updated on September 2016

A Pilot Study of Nocturnal Hypoglycemia Prevention in Type 1 Diabetes Using the Vigilant Diabetes Management Companion


Are you eligible to participate in this study?

You may be eligible for this study if you meet the following criteria:

  • Conditions: Diabetes Mellitus | Type 1 | Hypoglycemia
  • Age: Between 18 - 75 Years
  • Gender: Male or Female
  • Other:
    • Male or female participants aged between 18 and 75 years
    Clinical diagnosis of type 1 diabetes mellitus and using multiple daily
    injections or CSII for at least six months
    Patient has had documented nocturnal hypoglycemia in the last 2 months with an
    associated blood sugar reading less than 56mg/dL. Night is defined as the 8 hour
    interval when the patient usually sleeps (I.e. 11:00 pm to 7:00 am, for
    example).
    OR
    Patient has had at least 1 severe low at night in the last 6 months (helped by
    another). Night is defined as the 8 hour interval when the patient usually sleeps
    (I.e. 11:00 pm to 7:00 am, for example).
    Willing to monitor and record signs and symptoms of hypoglycemia
    Willing to test blood glucose levels at least three times a day
    Ability to use Android or IOS mobile phone
    No CGM Users

You may not be eligible for this study if the following are true:

  • • Pregnancy
    Unable to use the technology
    Any condition that in the investigators judgment is likely to cause the
    participant to be unable e to understand or provide informed consent
    Unwilling to use SMBG at least three times a day
    Unwilling to monitor and record signs and symptoms of hypoglycemia
    Individuals who are unwilling to share their glucose meter data

Recruitment Status: Open


Brief Description Eligibility Contact Research Team


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