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Clinical Trials in Canada / NCT06462170
Recruiting Not applicable

Pancreatic Insulin Production Capacity (PIPC) - a Feasibility Study

NCT06462170 · tracked via the Priya Life Science Canada tracker
Phase
Not applicable
Started
2024-06-24
Last updated
2026-05-06

Condition(s) studied

Type 2 Diabetes

Investigational drug(s) / intervention(s)

Boost Original meal replacement shake

Boost Original meal replacement shake: One bottle of Boost Original meal replacement shake.

Study summary

The standard treatment for Type 2 diabetes involves management of the disease based on average of blood glucose control over the past few months.

In this study, the investigators test for the participants' ability to produce insulin, which is the hormone that the body makes to control blood sugar levels. The body produces insulin in response to eating. The participants will drink a meal replacement shake, and then test the blood for levels of insulin produced over 2 hours.

With blood tests taken five times over two hours, the investigators will measure the blood glucose (sugar), and insulin levels. This study will assess the differences in insulin produced in the participants and try to understand the reasons for these differences.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. Consent provided 2. Age \>= 18 years. 3. Diagnosed as type 2 diabetes mellitus. 4. Not on insulin therapy. Exclusion Criteria: 1. Diagnosed as another form of diabetes mellitus. 2. Allergic to one or more ingredients in Boost meal replacement shake. 3. Unable to fast since midnight and attend in person for the morning protocol.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
The Ottawa Hospital Ottawa Ontario Recruiting

More Ottawa Hospital Research Institute trials in Canada

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06462170 on ClinicalTrials.gov ↗ ← All trials in Canada