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Prosective study on SGLT2i combined with theGLP-1RA in the treatment of Cardiovascular Kidney

Prosective study on SGLT2i combined with theGLP-1RA in the treatment of Cardiovascular Kidney

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600126712
Enrollment
Unknown
Registered
2026-06-14
Start date
2025-07-23
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

CKM syndrome

Interventions

Control group:None
Combination group:None

Sponsors

Zhongshan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. From July 22, 2025, to May 31, 2026, first-time prescriptions of GLP-1 receptor agonists (dulaglutide, exenatide, liraglutide, semaglutide) and/or SGLT-2 inhibitors (canagliflozin, dapagliflozin, empagliflozin, ertugliflozin). 2. Patients aged 18-75. 3. Patients meet the definition of cardiorenal metabolic syndrome, with distinctions made based on the disease stage of each patient.

Exclusion criteria

Exclusion criteria: 1. Patients previously diagnosed with type 1 diabetes; 2. Patients with contraindications to the study drug, such as end-stage kidney disease and multiple endocrine neoplasia; 3. Patients lacking important clinical data.

Design outcomes

Primary

MeasureTime frame
Major cardiovascular events (including cardiovascular death, non-fatal heart attack, and non-fatal stroke);Major kidney events (including eGFR drop >=50%, end-stage renal disease (ESRD), kidney-related death);

Secondary

MeasureTime frame
Adverse drug reactions;Hospitalization of heart failure;Fasting glucose;All cause death;Change rate of eGFR;Change of UACR;

Countries

China

Contacts

Public ContactQin Yan

Zhongshan Hospital, Fudan University

celeryan@163.com+86 21 64041990

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 29, 2026