Actively Recruiting

Age: 18Years +
All Genders
NCT07187830

Visceral Adipose Tissue and Liver Changes Associated With Semaglutide in CKD

Led by University of Alberta · Updated on 2026-05-11

52

Participants Needed

1

Research Sites

98 weeks

Total Duration

On this page

Sponsors

U

University of Alberta

Lead Sponsor

N

Novo Nordisk Canada Inc.

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Visceral Adipose Tissue and Liver Changes Associated With Semaglutide in CKD

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients 18 years of age or older
  • Diagnosed with type 2 diabetes for more than 18 months and chronic kidney disease in stages G1 to G4 based on KDIGO eGFR guidelines
  • Patients with type 2 diabetes and chronic kidney disease, regardless of semaglutide treatment status
  • Voluntary agreement to participate and signing informed consent
Not Eligible

You will not qualify if you...

  • Patients under 18 years of age
  • Pregnant, breastfeeding, planning pregnancy, or not using adequate contraception
  • Chronic kidney disease stage G5 or stage G4 requiring dialysis
  • Previous participation in this trial
  • Diagnosed neuropsychiatric diseases preventing understanding of study risks and benefits
  • Known or suspected allergy to trial medications or related products
  • Contraindications to study medications as stated in the Product Monograph
  • Refusal to participate or withdrawal of consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Mazankowski Alberta Heart Institute

Edmonton, Alberta, Canada, T6G 2B7

Actively Recruiting

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How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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