Looks at fat and liver changes in kidney patients taking semaglutide
Studies fat and liver changes in adults with kidney disease and diabetes.
Plain-language title generated from the registry record
Registry title: Visceral Adipose Tissue and Liver Changes Associated With Semaglutide in CKD
Key facts
- Where
- Edmonton, CanadaSee the site
AI summary: who the study is looking for
From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.
The trial is looking for adults with type 2 diabetes and chronic kidney disease, with or without semaglutide treatment, who attend diabetes clinics linked to the University of Alberta.
- Age
- 18 years or older
- Sex
- All sexes can join
- Disease stage
- Type 2 diabetes for more than 18 months and chronic kidney disease in stages G1, G2, G3a, G3b or G4
- Earlier treatment
- Can join with or without semaglutide treatment
- Biomarker or test result
- Kidney stage is set by eGFR: G1 is 90 or more, G2 is 60-89, G3a is 45-59, G3b is 30-44, G4 is 15-29
Main reasons for not taking part
- Under 18 years of age
- Pregnant, breastfeeding, planning pregnancy or not using adequate contraception
- Kidney disease stage G5, or stage G4 needing dialysis
- Neuropsychiatric disease that prevents understanding the study or choosing to join
- Known or suspected allergy to the trial medication or related products
Read by machine on 12 November 2026.
Where in Canada
- Mazankowski Alberta Heart InstituteEdmonton, CanadaContact: Ali SyedTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record → Contacts and Locations
Print a page for my doctorTrial details
- Who runs it
- University of Alberta
- Trial code
- NCT07187830
- Record updated
- 7 October 2026
- Original description
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.Read full original descriptionShow less
Region-specific Adipose Tissues and Liver Changes Associated With Semaglutide Treatment in Chronic Kidney Disease Patients
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.
Inclusion: 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.
Exclusion: Previous participation in this trial (screened or randomized); Contraindications to study medication(s), worded specifically as stated in the Product Monograph; Patients diagnosed with neuropsychiatric diseases that prevent them from understanding the benefits/risks associated with the project or voluntarily choosing to participate; Known or suspected allergy to trial medication(s), excipients, or related products; Patients <18 years of age; Pregnant, breastfeeding, or an intention of becoming pregnant or not using adequate contraceptive measures (including country-specific adequate measures, if any); Patients diagnosed with T2DM and CKD in stage G5 or stage G4 requiring dialysis as per KDIGO guidelines; Refusal to participate or consent revocation.