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Effects of SGLT2 Inhibition Treatment on Different Levels of Albuminuria in Patients With Type 2 Diabetes

Effects of SGLT2 Inhibition Treatment on Different Levels of Albuminuria in Patients With Type 2 Diabetes: a Prospective Interventional Study

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04127084
Enrollment
70
Registered
2019-10-15
Start date
2019-10-15
Completion date
2021-08-31
Last updated
2019-10-21

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

Conditions

Type 2 Diabetes, Diabetic Nephropathy

Keywords

Type 2 diabetes, Diabetic Nephropathy, Albuminuria, SGLT2 inhibitor

Brief summary

Diabetic kidney disease has become the leading cause for ESRD worldwide.Albuminuria is a major risk factor for progression of diabetic nephropathy. SGLT2 inhibitors are the first antiglycaemic drugs with direct renoprotection, which are thought to protect the kidneys by lowering albuminuria, stimulating urinary glucose excretion ,reducing systemic blood pressure, while simultaneously improving multiple other risk factors in a glucose-independent manner. However, the precise mechanisms behind the renal beneficial effect of SGLT2 inhibitors are not entirely elucidated, although ongoing outcome trials will confirm these findings. This study is to assess the impact of three months of treatment with SGLT2 Inhibitions on different levels of albuminuria in patients with type 2 diabetes and to evaluate the effects of SGLT2 inhibition treatment on markers for podocyte damage , renal fibrosis, inflammation,oxidative stress and renin-angiotensin- aldosterone system.

Detailed description

Objective: The primary objective is to assess the impact of three months of treatment with SGLT2 Inhibition on Different levels of Albuminuria in Patients With type 2 diabetes and to seek the relationship of this influences to relevant risk markers in the pathology of diabetic renal disease. Design: prospective ,intervention, case-controlled , single center study. Treatment period: 12 weeks. Patient population: 60 patients with type 2 diabetes recruited from Zhongshan Hospital Xiamen University in accordance with the study in- and exclusion criteria. Intervention: Dapagliflozine 10 mg once daily tablet treatment or Empagliflozin10 mg once daily tablet treatment or Canagliflozin 100 mg once daily tablet treatment. Endpoints: Primary outcome: evaluate the effects of SGLT2 inhibition treatment on on urinary albuminuria, kidney function and eGFR . Secondary endpoints To assess the effect of SGLT2 inhibition on markers for podocyte damage , renal fibrosis, inflammation,oxidative stress and renin-angiotensin- aldosterone system。 Timeframe: Recruiting planned from October 2019, inclusion over the following 12 months. Last patient is expected to be completed October 2020. Data analysis completed December 2020, publication autumn 2021.

Interventions

Dapagliflozine 5-10 mg once daily tablet treatment or Empagliflozin10 mg once daily tablet treatment or Canagliflozin 100 mg once daily tablet treatment

Sponsors

Zhongshan Hospital Xiamen University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. Male or female patients between 18 -80 years of age with a diagnosis of type 2 diabetes (WHO criteria). 2. HbA1c of 7-11 % 3. eGFR equal to or above 45 ml/min/1.73 m2 4. The Trial included 20 normal albuminuria (Urinary albumin creatinine ratio \[UACR\]\< 30 mg/g, with 20 moderately increased albuminuria UACR 30\ 300 mg/g, and 20 severely increased albuminuria UACR\>30 0mg/g (in ≥2 out 3 morning spot urine collections prior to enrolment ).at baseline. 5. Patients who agree to receive treatment with SGLT2 inhibitors. 6. Patients must be on current stable hemodynamic profile , without dehydration. 7. Patients must be on current stable antiglycaemic treatment with oral drugs (OAD) or insulin 4 weeks before start of study drug and throughout study duration. 8. Patients must be on stable antihypertensive treatment (not include renin-angiotensin system blocking treatment) 4 weeks before start of study drug and throughout study duration.

Exclusion criteria

1. type 1 diabetes 2. Patients who suffer from recent acute complications including diabetic ketoacidosis and hyperglycaemic hyperosmolar coma, which may be at risk for dehydration. 3. Patients with hypertension who are not on stable antihypertensive treatment 4. urinary tract or reproductive tract acute infection 5. impaired liver function, defined as aspartate aminotransferase (AST) \>3x upper limit of normal (ULN) and/or alanine aminotransferase (ALT) \>3x ULN 6. History of unstable or rapidly progressing renal disease 7. impaired renal function ,eGFR: \<45 mL/min (calculated by MDRD formula) 8. Ongoing cancer treatment 9. Recent Cardiovascular Events in a patient: 9.1. Acute Coronary Syndrome (ACS) within 2 months prior to enrolment 9.2.Hospitalization for unstable angina or acute myocardial infarction within 2 months prior to enrolment9. 3. Acute Stroke or TIA within two months prior to enrolment 9. 4. Less than two months post coronary artery revascularization 10. Congestive heart failure defined as New York Heart Association (NYHA) class IV, unstable or acute congestive heart failure.. 11. Pregnant or breastfeeding patients 12. smoker.

Design outcomes

Primary

MeasureTime frameDescription
changes of 8-OH-dGUp to 12 weeksTo evaluate the effects of SGLT2 inhibition treatment on oxidative stress index by detecting the levels of 8-OH-dG. Urinary 8-OH-dG concentrations were assayed using a competitive enzyme-linked immunosorbent assay
change in TGF-β1Up to 12 weeksTo assess effect of SGLT2 inhibition intervention on glomerular and tubulointerstitial fibrosis by detecting the expression of TGF-β1
change in IL-6Up to 12 weeksTo assess effect of SGLT2 inhibition intervention on inflammation biomarkers by detecting the levels of interleukin-6.
change in TNFαUp to 12 weeksTo evaluate the effects of SGLT2 inhibition treatment on inflammation, biomarkers by detecting the levels of tumor necrosis factor alpha.
changes of AGEsUp to 12 weeksTo evaluate the effects of SGLT2 inhibition treatment on oxidative stress index, the changes of AGEs.
Change in urinary albuminuriaUp to 12 weeksa clean-catch 24- hour urine sample and spot urine sample were collected to assess urinary albuminuria,which will be evaluated at week 0, and at end study week 12 (+/- 1 week)
Change in eGFRUp to 12 weekseGFR was calculated by modified glomerular filtration rate estimating equation for Chinese patients with chronic kidney disease.
change in nephrinUp to 12 weeksTo assess effect of SGLT2 inhibition intervention on glomerular podocyte injury by detecting the expression of renal nephrin.

Secondary

MeasureTime frameDescription
Change in aldosteroneUp to 12 weeksTo evaluate the levels of aldosterone before and after SGLT2 inhibition treatment.
Change in renninUp to 12 weeksTo evaluate the levels of rennin before and after SGLT2 inhibition treatment
Change in angiotensinUp to 12 weeksTo evaluate the levels of angiotensin before and after SGLT2 inhibition treatment
Change in uric acidUp to 12 weeksTo evaluate the levels of serum uric acid before and after SGLT2 inhibition treatment.

Countries

China

Contacts

Primary ContactXiao-min Chen, principal
chenxiaomin0517@sina.com8613860487599
Backup ContactYuan Tian, assistant
411954353@qq.com8618250865805

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 11, 2026