# Glucose-containing vs. glucose-free dialysate for patients with maintenance hemodialysis: Study protocol for a multicenter randomized controlled study-GLUMO study

**Authors:** Zhifeng Zhou, Qing Xu, Xin He, Santao Ou, Ling Zhang, Ahmet Murt, Ahmet Murt, Ahmet Murt, Ahmet Murt

PMC · DOI: 10.1371/journal.pone.0330155 · PLOS One · 2025-08-11

## TL;DR

This study will compare the safety and effectiveness of dialysate with and without glucose in patients undergoing regular hemodialysis.

## Contribution

The study introduces a large-scale RCT to evaluate the clinical impact of 5.5 mmol/L glucose-containing dialysate in hemodialysis.

## Key findings

- The study will assess the incidence of major cardiovascular and cerebrovascular adverse events.
- It will evaluate outcomes like hypoglycemia, hypotension, and blood pressure variability.
- Results will guide dialysate selection and improve dialysis prescriptions.

## Abstract

To mitigate the risk of infection and disordered blood lipid metabolism, glucose-free dialysate is widely utilized in China and European countries. While glucose-free dialysis does not necessarily lead to hypoglycemia, several other metabolic adjustments must occur to maintain normal blood glucose levels. Additionally, glucose-free dialysis may also increase the loss of amino acids and the susceptibility to hypotension and cardiovascular events. Incorporating an appropriate amount of glucose into the dialysate can help to offset the insufficient blood glucose during hemodialysis (HD), potentially reducing the incidence of hypoglycemia. Currently, the efficacy and safety of glucose-containing dialysate during HD remain contentious, and this study will be conducted to evaluate the efficacy and safety of 5.5 mmol/L glucose-containing dialysate for maintenance HD patients.

A multicenter, prospective, open-label, parallel-group, randomized controlled trial (RCT) will be conducted at more than 30 dialysis centers in China. Approximately 600 participants undergoing maintenance HD will be enrolled. Eligible patients will be randomly assigned to two groups, receiving either glucose-containing dialysate or glucose-free dialysate for HD at a 1:1 ratio, determined by a central computer-generated randomized sequence. The primary outcome is the incidence of the major cardiovascular and cerebrovascular adverse events (MACCE). Secondary outcomes are all-cause mortality, incidence of intradialytic hypotension (IDH), incidence of hypoglycemia, blood pressure and blood glucose variability, dysfunction of vascular access, cardiac function and fatigue level. Outcome assessors and data analysts will be blinded. All data will be analyzed using either intention-to-treat or per-protocol analysis methods.

The results of this study will provide evidence on the efficacy and safety of 5.5 mmol/L glucose-containing dialysate for maintenance HD patients, and will provide valuable insights for future dialysate selection and the enhancement of dialysis treatment prescriptions.

ChiCTR2400083153.

## Full-text entities

- **Diseases:** hypoglycemia (MESH:D007003), cardiovascular and cerebrovascular adverse (MESH:D002318), infection (MESH:D007239), hypotension (MESH:D007022), disordered blood lipid metabolism (MESH:D052439), fatigue (MESH:D005221)
- **Chemicals:** amino acids (MESH:D000596), blood glucose (MESH:D001786), Glucose (MESH:D005947)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12338788/full.md

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12338788/full.md

## References

29 references — full list in the complete paper: https://tomesphere.com/paper/PMC12338788/full.md

---
Source: https://tomesphere.com/paper/PMC12338788