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Comparison of the Efficacy and Safety of SGLT2i and GLP-1 Receptor Agonists in Obese Patients With Kidney Disease

Comparison of the Efficacy and Safety of Sodium-glucose Cotransporter 2 Inhibitors and Glucagon-like Peptide-1 Receptor Agonists in Obese Patients With Kidney Disease: a Single Center, Prospective, Exploratory Study

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06344247
Enrollment
48
Registered
2024-04-03
Start date
2023-09-01
Completion date
2025-12-01
Last updated
2024-04-03

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

Conditions

Chronic Kidney Diseases, Obesity

Keywords

Obesity, Chronic kidney disease, Sodium glucose cotransporter 2 inhibitors (SGLT2i), Glucagon like peptide-1 receptor agonists (GLP-1RA)

Brief summary

The goal of this clinical trial is to exploring the changes in 24-hour urinary protein and renal function in obese patients with kidney disease after the application of sodium glucose cotransporter 2 inhibitors (SGLT2i) and glucagon like peptide-1 receptor agonists (GLP-1RA). Eligible patients were randomly and non-blindly allocated to four groups in a 1:1:1:1 ratio.The first group is the optimized treatment group, and patients in this group maintain the maximum dose/maximum tolerated dose of RAS blocker therapy. The second group is the optimized treatment + SGLT2i group. Participants in this group are titrated to the target dose (10 mg qd) in combination with dapagliflozin on the basis of optimized treatment. The third group is the optimized treatment + GLP-1RA group. Participants in this group will be titrated to the target dose (1mg qw) in combination with semaglutide on the basis of optimized treatment. The last group is the optimized treatment + SGLT2i + GLP-1RA treatment group, that is, based on the optimized treatment, combined with dapagliflozin titrated to the target dose (10 mg qd) and semaglutide titrated to the target dose (1 mg qw).

Interventions

DRUGRAS inhibitors:Losartan®️/Valsartan®️

Losartan®️/Valsartan®️ : maintain the maximum dose/maximum tolerated dose.

DRUGdapagliflozin:Forxiga®️

Forxiga®️ : titrated to the target dose (10 mg qd).

DRUGsimagliptin:Forxiga®️

Semaglutide®️ : titrated to the target dose (1 mg qw).

Sponsors

RenJi Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

1. Agree to join this study and sign an informed consent form; 2. Age ≥ 18 years old and\<75 years old; 3. BMI ≥ 25kg/m ² Or waist circumference ≥ 85cm (male)/≥ 80cm (female) or waist to hip ratio ≥ 0.9 (male)/≥ 0.85 (female); 4. Confirmed obesity related kidney disease through renal biopsy within six months; 5. Have received optimized treatment with RAS blockers and/or MRA for at least 3 months;

Exclusion criteria

1. Diagnosed as secondary obesity, such as hypothyroidism, Cushing's syndrome, polycystic ovary syndrome, etc; 2. Severe renal insufficiency (renal function eGFR\<25 ml/min/1.73m2); 3. There is acute kidney injury; Defined as: (1) An increase in blood creatinine of ≥ 26.5 within 48 hours μ Mol/L; (2) Within 7 days, the increase in blood creatinine exceeds 1.5 times the baseline value or more; (3) Reduced urine output (\<0.5 ml/kg/h) and lasting for more than 6 hours. 4. Symptoms of active reproductive and urinary system infections 5. Severe liver dysfunction (ALT/AST greater than 2.5 times the upper normal limit); 6. Severe cardiovascular and cerebrovascular diseases, rheumatic and immune diseases; 7. Serious metabolic diseases, such as diabetes ketoacidosis, hypertonic hyperglycemia, etc; 8. Late stage malignant tumors; 9. Have a known history of using drugs that affect glucose and lipid metabolism, such as glucocorticoids, antibiotics, anti anxiety or antidepressants, etc; 10. Severe bleeding tendency and inability to complete venous blood collection; 11. There are contraindications for MRI examination, such as patients with pacemakers, nerve stimulators, artificial metal heart valves, etc; Patients with claustrophobia; Epilepsy patients, etc. 12. Pregnant/lactating women;

Design outcomes

Primary

MeasureTime frameDescription
Change of 24-hour urine protein quantification4、12、24、36、48 WEEKAccording to KDIGO 2021 glomerular disease management guidelines. ① Remission: proteinuria is reduced, and serum albumin is \>30g/L. Renal function is stable. Complete remission (CR): proteinuria is significantly reduced, 24HUTP\<0.3g/L, and serum albumin\>30g/L. Renal function is stable. Partial response (PR): proteinuria decreases, 24HUTP decreases \>50% from baseline and \>0.3g/L. Serum albumin\>30g/L. Renal function is stable. ② Invalid: proteinuria is not reduced compared with baseline, and serum albumin is \<30g/L. Renal function is stable or declining. ③Relapse: After achieving CR or PR, proteinuria increases (24-hour urine protein quantification ≥3.5g/d) and serum albumin decreases, \<30g/L. Renal function is stable or declining.

Secondary

MeasureTime frameDescription
Decline in glomerular filtration rate4、12、24、36、48 WEEK
Changes in BMI4、12、24、36、48 WEEKBody mass index
changes in fasting blood glucose4、12、24、36、48 WEEK

Countries

China

Contacts

Primary ContactQin Wang
qinwang_1975@126.com+8613621964604
Backup ContactWei Jin
jinwei_xj@126.com+8615026696535

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026