Actively Recruiting
Alleviating Carbohydrate Counting for Patients with Type-1 Diabetes Using a Closed Loop System with Weekly Subcutaneous Semaglutide
Led by McGill University Health Centre/Research Institute of the McGill University Health Centre · Updated on 2024-12-18
26
Participants Needed
1
Research Sites
108 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
A closed-loop insulin system, often labelled the "artificial pancreas" (AP), consists of an insulin pump, a continuous glucose monitor, and an interface coordinating between them to regulate insulin dosage based on glucose levels. Primarily designed for managing type 1 diabetes, this system has demonstrated significant benefits in previous studies. Yet, despite these advantages, certain challenges persist. Semaglutide, utilized in treating type 2 diabetes and obesity, is a once-weekly injectable medication that elevates levels of a gastrointestinal hormone known as Glucagon-Like Peptide-1 (GLP-1). This hormone alters gastric emptying, inhibits glucagon release, and reduces appetite. While not officially sanctioned for type 1 diabetes treatment in North America, studies have explored its efficacy as an adjunctive therapy alongside insulin, yielding favorable outcomes in blood glucose regulation. Comparable drugs like liraglutide and exenatide have been employed in type 1 diabetes treatment as well, albeit with less pronounced glucose-regulating effects compared to semaglutide, even in type 2 diabetes. The goal of this 50-week randomized placebo-controlled crossover 2x4 factorial designed trial is to assess whether commercial automated insulin delivery (AID) systems using rapid-acting insulin with adjunct weekly injections of semaglutide (at the maximally tolerated dose) can replace carbohydrate counting with simple meal announcements (SMA) without degrading glucose control.
CONDITIONS
Official Title
Alleviating Carbohydrate Counting for Patients with Type-1 Diabetes Using a Closed Loop System with Weekly Subcutaneous Semaglutide
Who Can Participate
Eligibility Criteria
You may qualify if you...
- At least 18 years of age
- Clinical diagnosis of type 1 diabetes for at least one year
- Use of a commercial advanced automated insulin delivery system for a minimum of 3 months
- Agreement to use effective birth control if of child-bearing potential (post-menarche females not menopausal and without medical sterility)
You will not qualify if you...
- Use of GLP-1 receptor agonists within the last 4 weeks
- Use of any anti-hyperglycemic medication other than insulin within the last 2 weeks
- Planned or ongoing pregnancy
- Breastfeeding
- Severe hypoglycemic episode in the last 3 months requiring emergency care or causing seizure or loss of consciousness
- Severe diabetic ketoacidosis within the last 6 months requiring medical attention and intravenous insulin
- History of acute or chronic pancreatitis or gallbladder disease
- Personal or family history of medullary thyroid cancer or multiple endocrine neoplasia type 2
- Severe kidney impairment with eGFR below 30 mL/min/1.73 m2 measured within the last 12 months
- Significant diabetic retinopathy or gastroparesis
- Bariatric surgery within the last 6 months
- Serious medical or psychiatric illness that may interfere with participation
- Body mass index of 21 kg/m2 or less
- Inability or unwillingness to safely manage diabetes during the study
- Safety concerns as judged by the primary investigator
AI-Screening
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Trial Site Locations
Total: 1 location
1
Research Institute of the McGill University Health Centre
Montreal, Quebec, Canada, H4A 3J1
Actively Recruiting
Research Team
G
Gabrielle Kemp, Registered Nurse
CONTACT
N
Nicholas Sabelli, B.Sc. (Hons)
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
QUADRUPLE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
TREATMENT
Number of Arms
2
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