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NCT06694558Recruiting

Monocytes in Subjects With Type 1 Diabetes and Chronic Kidney Disease

Source: ClinicalTrials.gov · Last updated 8 Jul 2026

Brief summary (registry, in English)

This is a cross-sectional study in patients with Type 1 diabetes (TID) and chronic kidney disease (CKD) to test if time in range (TIR) affects the degree of hyperglycemia required for monocyte activation, podocyte injury, and assess if monocyte activation is attenuated by glucagon-like peptide (GLP-1) agonist treatment ex vivo.

Status (registry)
Recruiting
Study type
Observational
Enrollment
60 (estimated)
First submitted
5 Nov 2024
Start date
1 Mar 2025
Primary completion date
30 Dec 2026
Lead sponsor
The Cleveland Clinic
NCT number
NCT06694558

What you commit to

  • Study type: Observational
  • Planned participants: 60
  • From 1 Mar 2025 to the primary completion date, 30 Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • On steroids
  • Reported heavy alcohol use or recreational drug use

Other illness

  • Diagnosed with cancer, immunosuppression/autoimmune conditions
  • Any condition which jeopardizes patient safety or affects monocytes at physician's discretion

Lab values

  • Hemoglobin \<9
  • On GLP-1 agonist or DPP4 inhibitor or sodium-glucose co-transporter-2 inhibitors use within 30 days

Other

  • pregnancy or plans to become pregnant

Who the study is looking for

  • T1D CKD subjects:
    • Adults, males or females diagnosed with T1D
    • Age 18-65 years
    • Diagnosed with CKD (eGFR 60-90 ml/min/1.73 m2)
    • Diagnosed with albuminuria (UACR 30-500 mg/g)
    • On insulin injections or pump
    • On CGM
    • Based on baseline CGM metrics, the investigators will stratify subjects to 2 groups Group A (Lower TIR group): TIR\<60%, A1c 7.5-9.5 Group B (Higher TIR group): TIR\>70% A1c 5.0-7.0
  • Controls: T1D subjects without CKD
    • Adults, males or females diagnosed with T1D
    • Age 18-65 years
    • No CKD (eGFR \>90 ml/min/1.73 m2)
    • No albuminuria (UACR \<30 mg/g)
    • On insulin injections or pump
    • On CGM
    • Based on baseline CGM metrics, the investigators will stratify subjects to 2 groups Group A (Lower TIR group): TIR\<60%, A1c 7.5-9.5 Group B (Higher TIR group): TIR\>70% A1c 5.0-7.0

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Cleveland Clinic
Coordinator of this site? Confirm its status
ClevelandUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.