Maintenance Notice

Due to necessary scheduled maintenance, the JMIR Publications website will be unavailable from Wednesday, July 01, 2020 at 8:00 PM to 10:00 PM EST. We apologize in advance for any inconvenience this may cause you.

Who will be affected?

Accepted for/Published in: JMIR Research Protocols

Date Submitted: Jan 4, 2024
Date Accepted: Apr 25, 2024
Date Submitted to PubMed: Apr 29, 2024

The final, peer-reviewed published version of this preprint can be found here:

Effects of Empagliflozin in Type 2 Diabetes With and Without Chronic Kidney Disease and Nondiabetic Chronic Kidney Disease: Protocol for 3 Crossover Randomized Controlled Trials (SiRENA Project)

Nielsen SF, Duus CL, Buus NH, Bech JN, Mose FH

Effects of Empagliflozin in Type 2 Diabetes With and Without Chronic Kidney Disease and Nondiabetic Chronic Kidney Disease: Protocol for 3 Crossover Randomized Controlled Trials (SiRENA Project)

JMIR Res Protoc 2024;13:e56067

DOI: 10.2196/56067

PMID: 38680116

PMCID: 11170048

Empagliflozin in type 2 diabetes with and without CKD and non-diabetic CKD: Protocol for 3 randomized, double-blind, placebo controlled cross-over trials -The SiRENA project

  • Steffen Flindt Nielsen; 
  • Camilla Lundgreen Duus; 
  • Niels Henrik Buus; 
  • Jesper Nørgaard Bech; 
  • Frank Holden Mose

ABSTRACT

Background:

Sodium-Glucose-Cotransporter 2 inhibitors (SGLT2i) have revolutionized treatment of type 2 diabetes mellitus (DM2) and chronic kidney disease (CKD), reducing risk of cardiovascular and renal endpoints by up to 40%. The underlying mechanisms are not fully understood.

Objective:

To examine the effects of empagliflozin versus placebo on renal hemodynamics, sodium balance, vascular function, and markers of the innate immune system in patients with DM2, DM2 and CKD and non-diabetic CKD.

Methods:

We conducted three randomized, double-blind, placebo controlled cross over trials, each with identical study protocol but different study populations. We included patients with DM2 and preserved kidney function (estimated glomerular filtration rate (eGFR) > 60 ml/min/1.73 m2), DM2 and CKD and non-diabetic CKD (both with eGFR 20-60 ml/min/1.73 m2). Each participant was randomly assigned to four weeks of treatment with either empagliflozin 10 mg once daily or matching placebo. After a wash-out period of at least two weeks, participants were crossed over to the opposite treatment. Endpoints were measured at the end of each treatment period. The primary endpoint was renal blood flow (RBF) measured with 82Rubidium positron emission tomography/ computed tomography (82Rb-PET/CT). Secondary endpoints include glomerular filtration rate (GFR) measured with 99mTechnetium- diethylene-triamine-pentaacetate (99mTc-DTPA) clearance, vascular function assessed by forearm venous occlusion strain gauge plethysmography, measurements of the nitric oxide (NO)-system, water and sodium excretion, body composition measurements and markers of the complement immune system.

Results:

Recruitment began in April 2021 and was completed in September 2022. Examinations were completed by December 2022. 49 participants completed the project; 16 in the DM2 and preserved kidney function study, 17 in the DM2 and CKD study and 16 in the non-diabetic CKD study. Data analysis is ongoing. Results are yet to be published.

Conclusions:

This article describes the rationale, design and methods used in a project consisting of three randomized, double-blind, placebo controlled cross over trials examining the effects of empagliflozin versus placebo in patients with DM2 with and without CKD and patients with non-diabetic CKD, respectively. Clinical Trial: EU Clinical Trials Register 2019-004303-12, 2019-004447-80 and 2019-004467-50


 Citation

Please cite as:

Nielsen SF, Duus CL, Buus NH, Bech JN, Mose FH

Effects of Empagliflozin in Type 2 Diabetes With and Without Chronic Kidney Disease and Nondiabetic Chronic Kidney Disease: Protocol for 3 Crossover Randomized Controlled Trials (SiRENA Project)

JMIR Res Protoc 2024;13:e56067

DOI: 10.2196/56067

PMID: 38680116

PMCID: 11170048

Download PDF


Request queued. Please wait while the file is being generated. It may take some time.

© The authors. All rights reserved. This is a privileged document currently under peer-review/community review (or an accepted/rejected manuscript). Authors have provided JMIR Publications with an exclusive license to publish this preprint on it's website for review and ahead-of-print citation purposes only. While the final peer-reviewed paper may be licensed under a cc-by license on publication, at this stage authors and publisher expressively prohibit redistribution of this draft paper other than for review purposes.