Type 2 Diabetes (T2D) Clinical Trials

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Region-specific Adipose Tissues and Liver Changes Associated With Semaglutide Treatment in Chronic Kidney Disease Patients

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

Obesity is considered a global pandemic and is associated with various diseases and metabolic complications, such as type 2 diabetes mellitus, high blood pressure, cholesterol disorders, cancer, cardiovascular disease, and kidney disease. Obesity can affect the kidneys in two main ways: indirectly, through mechanisms related to diabetes mellitus and/or high blood pressure, and directly, through complex proteins called adipokines, which are produced by adipocytes. Many of these adipokines are secreted by adipocytes under normal conditions, as they contribute to maintaining immune defenses and energy production. However, in obesity these adipokines acquire harmful properties and produce chronic inflammation in vital organs, such as the heart, blood vessels, the pancreas, and the kidney, leading to a deterioration in liver and kidney function. New drugs such as glucagon-like peptide-1 receptor agonists (GLP-1Ras / Semaglutide), are not only effective to regulate blood sugar levels, but they produce weight loss improving kidney and liver function. However, little is known about their specific effect on the adipose tissue. Therefore, studies focusing on how these drugs work in fat could help us understand how diseased adipose tissue can affect patients with heart, liver, and kidney disease. Investigators are asking patients who attend the diabetes clinics associated with the University of Alberta to join the study.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patients ≥ 18 years of age.

• Patients diagnosed with T2DM (\>18 months) and CKD in stages G1, G2, G3a, G3b and G4; the CKD staging will be established according to the eGFR as per the KDIGO guidelines (G1: eGFR ≥90 ml/min/1.73m2; G2: 60-89 ml/min/1.73m2; G3a: 45-59 ml/min/1.73m2; G3b: 30-44 ml/ min/1.73m2; G4: 15-29 ml/ min/1.73m2).

• Patients with T2DM and CKD, with or without semaglutide treatment.

• Patients who voluntarily agree to participate and sign informed consent.

Locations
Other Locations
Canada
Mazankowski Alberta Heart Institute
RECRUITING
Edmonton
Time Frame
Start Date: 2026-02-23
Estimated Completion Date: 2028-01-15
Participants
Target number of participants: 52
Treatments
No semaglutide
Patients with diabetes not treated with semaglutide
Semaglutide
Patients with diabetes receiving semaglutide
Sponsors
Collaborators: Novo Nordisk Canada Inc.
Leads: University of Alberta

This content was sourced from clinicaltrials.gov