Clinical trial Recruiting at 1 site Observational Ages 18 to 90

How GLP‑1 receptor agonists affect unhealthy organ fat in people with chronic kidney disease

Official title: Clinical, Morphometric and Biochemical Effects on Adiposopathy Associated With the Use of GLP-1 Receptor Agonists in Chronic Kidney Disease

Run by Cardenal Herrera University · NCT07309094 · Data updated 2026-11-12

This observational project will test whether taking GLP‑1 receptor agonist medicines changes harmful fat around organs and related inflammation in adults with chronic kidney disease who also have obesity or type 2 diabetes.

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Quick facts

Study typeObservational
Ages18 Years to 90 Years
SexAll
Enrollment250 (estimated)
SponsorCardenal Herrera University
Academic / other
Locations1 site (Valencia, Valencia)
StatusRecruiting
StartedSeptember 15, 2023
Main results expectedJuly 31, 2027
Study endsDecember 31, 2028
Registry record updatedDecember 30, 2025
Trial IDNCT07309094 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 18 or older with chronic kidney disease stages G1–G4 (not on dialysis) who have uncontrolled type 2 diabetes, obesity, and/or cardiovascular disease and who can give informed consent are appropriate candidates.

Probably not a fit

People with end‑stage CKD (stage G5) or candidates for dialysis, pregnant individuals, or those with neuropsychiatric conditions preventing informed consent are unlikely to benefit from participation.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is an observational cohort study that follows adults with CKD stages G1–G4, comparing those treated with GLP‑1 receptor agonists to those not receiving these drugs while recording other glucose‑lowering therapies. Investigators will use imaging (CT/MRI), bioimpedance, morphometric measures, and blood biomarkers to quantify perivisceral adipose tissue, radiodensity, and pro‑inflammatory adipokines alongside kidney function measures. The study documents real‑world use of GLP‑1RAs, SGLT2 inhibitors, tirzepatide and other medications rather than assigning treatments. Data will be analyzed to link changes in adipose tissue characteristics with biochemical markers and clinical measures of kidney and cardiovascular risk.

Why it matters

Potential benefit: If successful, the findings could show that GLP‑1RAs reduce harmful periorgan fat and inflammation, which might help slow CKD progression and lower cardiovascular risk.

How similar studies have gone: Previous randomized and observational studies have shown renal and cardiovascular benefits of GLP‑1RAs in people with type 2 diabetes and obesity, but direct, detailed links between GLP‑1RA use and improvements in perivisceral adiposopathy remain less well established.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* \> or = 18 years of age
* diagnosed with CKD in stages G1, G2, G3a, G3b, and G4, not candidate for dialysis
* had uncontrolled T2DM, CVDs and/or obesity
* willing to participate in the study and sign informed consent

Exclusion Criteria:

* Age \<18 years
* pregnancy
* CKD in stage G5 or G4 candidate for dialysis
* neuropsychiatric diseases preventing the patient from understanding the benefits/risks associated with the project
* refusal to participate and/or consent revocation were considered as exclusion criteria

Where it's running

  • Vithas Valencia Consuelo
    Valencia, Valencia, Spain
    Recruiting

Study contacts

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.