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NCT07094529Recruiting

Personalized Hypoglycemia Outpatient Treatment - a Feasibility Study

The Feasibility of Personalized Hypoglycemia Outpatient Treatment for People Living With Type 2 Diabetes Mellitus

Source: ClinicalTrials.gov · Last updated 30 Jul 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

This study will offer two study interventions designed to bring on a mild low blood sugar (capillary blood glucose result 3.0 to 3.8 mmol/L), in order to study the effectiveness of each study participant's personal choice of treatment and first recheck time. The two study interventions that the participant can choose to complete (one or both interventions). Based on each participant's own experience with hypoglycemia treatment or their preferences, the participant can choose one of 4 simple carbohydrate treatment quantities, and choose one of 4 capillary blood glucose recheck times.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
120 (estimated)
First submitted
21 Jul 2025
Start date
Jul 2025
Primary completion date
Dec 2026
Lead sponsor
Ottawa Hospital Research Institute
NCT number
NCT07094529

What you commit to

  • Study type: Interventional
  • Planned participants: 120
  • From Jul 2025 to the primary completion date, Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Lab values

  • An individual who meets any of the following criteria will be excluded from participation in this study:
    • Diagnosed as another form of diabetes mellitus.
    • Has a history of hypoglycemia unawareness.
    • Had a hypoglycemia event, defined as capillary blood glucose \< 3.9 mmol/L within 24 hours prior to the study visit booking time.

Who the study is looking for

  • In order to be eligible to participate in this study, an individual must meet all of the following criteria:
    • Consent provided
    • Age \>= 18 years.
    • Diagnosed as type 2 diabetes mellitus.
    • Type 2 diabetes medications include at least one of the following for at least one month prior to entering the study: sulfonylurea or insulin of any type.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
The Ottawa Hospital
Coordinator of this site? Confirm its status
OttawaCanadaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.