Monocytes in Subjects With Type 1 Diabetes and Chronic Kidney Disease

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

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
View:

• 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

Locations
United States
Ohio
Cleveland Clinic
RECRUITING
Cleveland
Contact Information
Primary
Andrea Debs
debsa@ccf.org
216-445-8354
Time Frame
Start Date: 2025-03-01
Estimated Completion Date: 2026-07-01
Participants
Target number of participants: 60
Treatments
Patients with Type 1 Diabetes
Patients with Type 1 Diabetes with or without chronic kidney disease
Related Therapeutic Areas
Sponsors
Collaborators: National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), Stanford University
Leads: The Cleveland Clinic

This content was sourced from clinicaltrials.gov