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A Real-World Study of SGLT2 Inhibitors in Very Elderly Patients with Multiple Comorbidities

A Real-World Study of SGLT2 Inhibitors in Very Elderly Patients with Multiple Comorbidities

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600119830
Enrollment
Unknown
Registered
2026-03-04
Start date
2026-03-04
Completion date
Unknown
Last updated
2026-03-09

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

Conditions

Chronic heart failure, chronic kidney disease (stages 3–4), type 2 diabetes, atherosclerotic cardiovascular disease (coronary heart disease, ischemic stroke, peripheral artery disease)

Interventions

Non-SGLT2i Control Group:NA
SGLT2 Inhibitor Group:NA

Sponsors

Xi'an Jiaotong University Second Affiliated Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
80 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged >=80 years at the index date. 2. Meet the definition of "multiple comorbidities": The patient must have been clinically diagnosed with >=2 diseases from the following core chronic disease list during the index hospitalization, with at least one being the primary reason for this hospitalization or directly related to decompensation: Type 2 diabetes (currently receiving glucose-lowering treatment or HbA1c >=7.0%) Chronic heart failure (NYHA class II–IV, or with recent evidence of decompensation) Chronic kidney disease (CKD stages 3–4, baseline eGFR 25–90 mL/min/1.73m²) Atherosclerotic cardiovascular disease (coronary heart disease, ischemic stroke, peripheral artery disease); 3. Hospitalization due to acute decompensation or complications of diseases listed above, and discharged alive. 4. During this hospitalization or at discharge, newly prescribed any SGLT2 inhibitor (SGLT2i group), or not prescribed an SGLT2i but receiving guideline-recommended standard treatment for the primary diagnosis (control group). 5. Baseline eGFR >=25 mL/min/1.73m².

Exclusion criteria

Exclusion criteria: 1. Any use of SGLT2 inhibitors within 365 days prior to the index date. 2. Type 1 diabetes mellitus. 3. End-stage renal disease at the index date (eGFR <15 mL/min/1.73m² or receiving renal replacement therapy). 4. Life expectancy <3 months at the index date. 5. Key information in the medical records (such as discharge medications and primary endpoints) is severely missing, making it impossible to assign groups or determine endpoints.

Design outcomes

Primary

MeasureTime frame
The composite cardiorenal outcome occurring within one year after discharge.;

Secondary

MeasureTime frame
Composite safety endpoint;Medication patterns;

Countries

China

Contacts

Public ContactGaigai Ma

Xi'an Jiaotong University Second Affiliated Hospital

magaigai@xjtu.edu.cn+86 29 86320430

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 14, 2026