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Continuous Glucose Monitoring in People With Diabetes on Dialysis

Real-World Evaluation of Continuous Glucose Monitoring Data in People With Diabetes and End-Stage Renal Disease Receiving Dialysis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06657508
Acronym
RECORD
Enrollment
40
Registered
2024-10-24
Start date
2024-12-31
Completion date
2030-10-01
Last updated
2026-04-29

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

Conditions

Diabetes Mellitus, End-Stage Renal Disease

Keywords

Diabetes mellitus, End-stage renal disease, End-stage kidney disease, Dialysis, Haemodialysis, Peritoneal dialysis, Kidney replacement therapy, Continuous Glucose Monitoring, Glucose fluctuations

Brief summary

Continuous glucose monitoring is a sensor, which monitors glucose levels continuously throughout the day. In people with diabetes, especially those treated with insulin, this sensor helps guide the amount of treatment (such as insulin) required to maintain glucose within target. In dialysis, the glucose levels and insulin needs can change a lot because of the kidney failure and dialysis treatments. The goal of this observational study is to describe the changes in glucose during and in between dialysis sessions over two weeks by using continuous glucose monitoring. The study will also explore whether there is a relationship between the trend of the glucose and fluid level changes during and in between dialysis treatments. Also, the study will assess whether there is a relationship between glucose levels and several long-term outcomes, such as admissions to the hospital, for up to five years.

Detailed description

This is a single-centre observational prospective study, which involves existing users of NHS funded continuous glucose monitoring (CGM) with insulin-treated diabetes mellitus (DM) and end-stage renal disease (ESRD) established on dialysis. CGM is the standard of care for glucose monitoring in all people with type 1 DM and specific groups with type 2 DM in the United Kingdom. The study aims to evaluate the association between glucose levels in people with diabetes who are on dialysis with short- and long-term clinical outcomes. The study will address the following hypotheses: 1. Dialysis causes fluctuation in CGM glucometrics during dialysis and in between dialysis periods. 2. Dysglycaemia is associated with adverse short- and long-term outcomes in people with diabetes who are on dialysis. The primary objective of the study is to describe glucose levels in the intradialytic and interdialytic periods, by accessing CGM-derived glucometrics over 2 weeks. The secondary objectives of the study are as follows: Short term outcomes: * To understand the impact of dialysis on CGM glucometrics in intradialytic and interdialytic periods (maintenance haemodialysis or peritoneal dialysis) by using raw glucose data combined across multiple different sensors * To investigate the association of glycaemic control (CGM data and HbA1c) with: * Ultrafiltration volume (assessed via body weight change in the intradialytic period) * Body composition (assessed by bioelectrical impedance analysis) * Blood pressure Long term outcomes: * To investigate the association of CGM metrics (intradialytic and interdialytic periods and 14- and 90-day data) and HbA1c with long term outcomes (up to 5 years): * Mortality * Hospital admissions * Cardiovascular events (acute myocardial infarction, stroke, acute or decompensated heart failure) * New diabetic foot ulcer or peripheral vascular disease requiring intervention or amputations * To compare CGM measures with HbA1c as a predictor of long-term outcomes as described above

Interventions

None listed

Sponsors

University of Nottingham
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* Age: ≥18 years (no upper age limit) * People with insulin-treated diabetes who receive NHS funded continuous glucose monitoring as part of their routine clinical care * Diabetes duration \> 6 months * People with end-stage renal disease established on dialysis (maintenance haemodialysis or peritoneal dialysis) * Ability to give informed consent

Exclusion criteria

* Participation in other competing studies/clinical trials as determined by the study investigator * Serious illness or events with life expectancy \< 3 months or other significant illness which, in the opinion of the study clinician, precludes involvement

Design outcomes

Primary

MeasureTime frame
Change in continuous glucose monitoring % time in glucose range [3.9-10.0 mmol/l] between intradialytic and interdialytic periodsFrom baseline to 2 weeks, over 6 consecutive dialysis sessions

Secondary

MeasureTime frameDescription
Change in continuous glucose monitoring % time in tight glucose range [3.9-7.8 mmol/l] between intradialytic and interdialytic periodsFrom baseline to 2 weeks, over 6 consecutive dialysis sessions
Change in continuous glucose monitoring % time above glucose range, level 1 [10.1-13.9 mmol/L] between intradialytic and interdialytic periodsFrom baseline to 2 weeks, over 6 consecutive dialysis sessions
Change in continuous glucose monitoring % time above glucose range, level 2 [>13.9 mmol/l] between intradialytic and interdialytic periodsFrom baseline to 2 weeks, over 6 consecutive dialysis sessions
Change in continuous glucose monitoring % time below glucose range, level 1 [3.0-3.8 mmol/l] between intradialytic and interdialytic periodsFrom baseline to 2 weeks, over 6 consecutive dialysis sessions
Change in continuous glucose monitoring % time below glucose range, level 2 [<3.0 mmol/l] between intradialytic and interdialytic periodsFrom baseline to 2 weeks, over 6 consecutive dialysis sessions
Change in continuous glucose monitoring average glucose between intradialytic and interdialytic periodsFrom baseline to 2 weeks, over 6 consecutive dialysis sessions
Change in continuous glucose monitoring % coefficient of variation between intradialytic and interdialytic periodsFrom baseline to 2 weeks, over 6 consecutive dialysis sessions
Change in continuous glucose monitoring Glucose management indicator (GMI) between intradialytic and interdialytic periodsFrom baseline to 2 weeks, over 6 consecutive dialysis sessions
Relationship between continuous glucose monitoring metrics and baseline Gold scoreFrom baseline to 2 weeks, over 6 consecutive dialysis sessionsThe Gold score assesses hypoglycaemia awareness
Relationship between continuous glucose monitoring metrics and baseline Diabetes Distress Scale [DDS-17] scoreFrom baseline to 2 weeks, over 6 consecutive dialysis sessions
Relationship between continuous glucose monitoring metrics and baseline Problem Areas in Diabetes [PAID] scoreFrom baseline to 2 weeks, over 6 consecutive dialysis sessions
Relationship between continuous glucose monitoring metrics and baseline Glucose Monitoring Satisfaction Survey [GMSS] scoreFrom baseline to 2 weeks, over 6 consecutive dialysis sessions
Relationship between continuous glucose monitoring metrics and baseline Hypoglycaemia Fear Survey-Version II Worry scale [HFS-II W] scoreFrom baseline to 2 weeks, over 6 consecutive dialysis sessions
Relationship between continuous glucose monitoring metrics and baseline Integrated Palliative Outcome Score [IPOS]-renal scoreFrom baseline to 2 weeks, over 6 consecutive dialysis sessions
Relationship between continuous glucose monitoring metrics and baseline Dialysis Thirst Inventory questionnaire scoreFrom baseline to 2 weeks, over 6 consecutive dialysis sessions
Relationship between glucose outcomes and body composition measures on dialysis days assessed by bioelectrical impedance analysisFrom baseline to 2 weeks, over 6 consecutive dialysis sessionsGlucose outcomes include 14- and 90- day continuous glucose monitoring metrics at baseline, intradialytic and interdialytic continuous glucose monitoring metrics, baseline HbA1c
Relationship between glucose outcomes and ultrafiltration volume during dialysis sessions assessed via body weight changes in the intradialytic periodFrom baseline to 2 weeks, over 6 consecutive dialysis sessionsGlucose outcomes include 14- and 90- day continuous glucose monitoring metrics at baseline, intradialytic and interdialytic continuous glucose monitoring metrics, baseline HbA1c
Relationship between glucose outcomes and changes in blood pressure in the intradialytic periodFrom baseline to 2 weeks, over 6 consecutive dialysis sessionsGlucose outcomes include 14- and 90- day continuous glucose monitoring metrics at baseline, intradialytic and interdialytic continuous glucose monitoring metrics, baseline HbA1c. Changes in blood pressure are assessed by measuring blood pressure prior to and post dialysis sessions
Association between glucose outcomes and mortalityFrom baseline to 5 yearsGlucose outcomes include 14- and 90- day continuous glucose monitoring metrics at baseline, baseline HbA1c, intradialytic and interdialytic continuous glucose monitoring metrics, 14- and 90- day continuous glucose monitoring metrics and HbA1c at month 3, 6, 9 and 12
Association between glucose outcomes and hospital admissionsFrom baseline to 5 yearsGlucose outcomes include 14- and 90- day continuous glucose monitoring metrics at baseline, baseline HbA1c, intradialytic and interdialytic continuous glucose monitoring metrics, 14- and 90- day continuous glucose monitoring metrics and HbA1c at month 3, 6, 9 and 12
Association between glucose outcomes and cardiovascular outcomesFrom baseline to 5 yearsGlucose outcomes include 14- and 90- day continuous glucose monitoring metrics at baseline, baseline HbA1c, intradialytic and interdialytic continuous glucose monitoring metrics, 14- and 90- day continuous glucose monitoring metrics and HbA1c at month 3, 6, 9 and 12. Cardiovascular outcomes include acute myocardial infarction, stroke, acute or decompensated heart failure
Association between glucose outcomes and new diabetic foot ulcer requiring intervention or amputationFrom baseline to 5 yearsGlucose outcomes include 14- and 90- day continuous glucose monitoring metrics at baseline, baseline HbA1c, intradialytic and interdialytic continuous glucose monitoring metrics, 14- and 90- day continuous glucose monitoring metrics and HbA1c at month 3, 6, 9 and 12
Association between glucose outcomes and new peripheral vascular disease requiring intervention or amputationFrom baseline to 5 yearsGlucose outcomes include 14- and 90- day continuous glucose monitoring metrics at baseline, baseline HbA1c, intradialytic and interdialytic continuous glucose monitoring metrics, 14- and 90- day continuous glucose monitoring metrics and HbA1c at month 3, 6, 9 and 12

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 30, 2026