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Efficacy and safety of Finerenone in patients with type 2 diabetes mellitus combined with chronic kidney disease in a "in person-remote" diabetes mellitus self-management support model: a single-center retrospective real-world study

Efficacy and safety of Finerenone in patients with type 2 diabetes mellitus combined with chronic kidney disease in a "in person-remote" diabetes mellitus self-management support model: a single-center retrospective real-world study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400087169
Enrollment
Unknown
Registered
2024-07-22
Start date
2024-08-01
Completion date
Unknown
Last updated
2024-07-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Type 2 Diabetes Mellitus

Interventions

Finerenone intervention group:Continuous application of Finerenone for at least 3 months at the Diabetes Shared Care Real World Management Follow-Up
Type 2 diabetes combined with CKD control group:CKD adjudicated at the Diabetes Shared Care Real World Management Follow-Up, but not clinically applied Finerenone

Sponsors

Peking University First Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients in the diabetes shared care management cohort of Peking University First Hospital who completed the initial registration from October 2016 to February 2024 2. Patients with type 2 diabetes; 3. Aged >18 years; 4. Patients with a clinical diagnosis of diabetic nephropathy and UACR =30mg/g

Exclusion criteria

Exclusion criteria: 1. Patients who, as of February 2024, have been withdrawn from follow-up in the diabetes shared care outpatient management cohort for various reasons; 2. Patients with non-type 2 diabetes such as pre-diabetes, type 1 diabetes, and specific types of diabetes 3. Patients with a clinical or renal puncture diagnosis of non-diabetic nephropathy.

Design outcomes

Primary

MeasureTime frame
Change of Urinary microalbumin creatinine ratio from baseline at 3-6 months of Finerenone treatment;

Secondary

MeasureTime frame
Change of Estimated glomerular filtration rate and Serum potassium from baseline at 3-6 months of Finerenone treatment;Change of Urinary microalbumin creatinine ratio, Estimated glomerular filtration rate and Serum potassium from baseline at 3-6 months of Finerenone treatment combine/or SGLT-2i treatment;Change of Urinary microalbumin creatinine ratio, Estimated glomerular filtration rate and Serum potassium from baseline at 3-6 months of Finerenone treatment in Patients with different proteinuria levels;Change of Urinary microalbumin creatinine ratio, Estimated glomerular filtration rate and Serum potassium from baseline at 3-6 months of Finerenone treatment in Patients with different CKD duration;

Countries

China

Contacts

Public ContactLi Ang

Peking University First Hospital

liang850513@hotmail.com+86 136 8133 8795

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026