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Assessment of the Accuracy of Continuous Glucose Sensors in People With Diabetes Undergoing Haemodialysis (ALPHA)

Primary Purpose

Diabetic Nephropathies, Type 1 Diabetes Mellitus, Chronic Kidney Diseases

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Dexcom G6 and Abbott Freestyle Libre
Sponsored by
Imperial College London
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Diabetic Nephropathies focused on measuring Type 1 Diabetes Mellitus, Chronic Kidney Diseases

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Adults >18 years of age
  • Diabetes, with insulin treatment for over 6 months or on sulphonylureas
  • Chronic kidney disease requiring haemodialysis three times per week

Exclusion Criteria:

  • Pregnant or planning pregnancy
  • Breastfeeding
  • Enrolled in other clinical trials
  • Have active malignancy or under investigation for malignancy
  • Severe visual impairment
  • Reduced manual dexterity
  • Unable to participate due to other factors, as assessed by the Chief Investigators

Sites / Locations

  • Imperial College London/NHS trust Renal Unit

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Dexcom G6 and Abbott Freestyle Libre

Arm Description

Participants will have a Dexcom G6 sensor and Abbott FreeStyle Libre sensor inserted in the abdomen and upper arm respectively. Participants will be asked to swipe the FreeStyle Libre reader across the sensor a minimum of every 8 hours. Participants will be asked to continue their usual regimen of self-monitoring capillary blood glucose (SMBG). During haemodialysis, a dialysis circuit blood sample will be drawn at 0 (pre-dialysis) 30, 60, 90, 120, 150, 180, 210 and 240 minutes and immediately after dialysis. Samples from the circuit will be analysed on the YSI glucose analyser. Participants will be asked to change the FreeStyle Libre sensors at day 14. The blinded CGM data will be uploaded at the time of each sensor change by the research team.

Outcomes

Primary Outcome Measures

MARD between G6 and YSI
Mean absolute relative difference between Dexcom G6 and YSI glucose during haemodialysis
MARD between Libre and YSI
Mean absolute relative difference between Dexcom G6 and YSI glucose during haemodialysis

Secondary Outcome Measures

HbA1c
Glycated Haemoglobin
MARD for G6 and YSI <3.9mmol/L
Mean absolute relative difference between Dexcom G6 and YSI glucose <3.9mmol/L
MARD for Libre and YSI <3.9mmol/L
Mean absolute relative difference between Libre and YSI glucose <3.9mmol/L
MARD for Libre and YSI 3.9-10mmol/L
Mean absolute relative difference between Libre and YSI glucose 3.9-10mmol/L
MARD for Libre and YSI >10mmol/L
Mean absolute relative difference between Libre and YSI glucose >10mmol/L
MARD for G6 and YSI 3.9-10mmol/L
Mean absolute relative difference between Dexcom G6 and YSI glucose 3.9-10mmol/L
MARD for G6 and YSI >10mmol/L
Mean absolute relative difference between Dexcom G6 and YSI glucose >10mmol/L
MARD for G6 and YSI 24hr pre
Mean absolute relative difference between Dexcom G6 and YSI glucose during 24 hours prior to heamodialysis
MARD for Libre and YSI 24hr pre
Mean absolute relative difference between Libre and YSI glucose during 24 hours prior to heamodialysis
MARD for Libre and YSI 24hr post
Mean absolute relative difference between Libre and YSI glucose during 24 hours after heamodialysis
MARD for G6 and YSI 24hr post
Mean absolute relative difference between Dexcom G6 and YSI glucose during 24 hours after heamodialysis
CEG analysis G6 and YSI
Clarke Error Grid analysis between Dexcom G6 and YSI glucose during haemodialysis
CEG analysis Libre and YSI
Clarke Error Grid analysis between Libre and YSI glucose during haemodialysis
Severe hypoglycaemia
Episodes of severe hypoglycaemia
DKA
Diabetic Ketoacidosis
Sensor failure
Events of G6/libre sensor failure
Missing glucose data
Missing blood glucose data for G6/libre measured by number of missing data points

Full Information

First Posted
February 22, 2019
Last Updated
August 4, 2022
Sponsor
Imperial College London
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1. Study Identification

Unique Protocol Identification Number
NCT03885362
Brief Title
Assessment of the Accuracy of Continuous Glucose Sensors in People With Diabetes Undergoing Haemodialysis
Acronym
ALPHA
Official Title
Assessment of the Accuracy of Continuous Glucose Sensors in People With Diabetes Undergoing Haemodialysis
Study Type
Interventional

2. Study Status

Record Verification Date
August 2022
Overall Recruitment Status
Completed
Study Start Date
December 11, 2019 (Actual)
Primary Completion Date
July 1, 2022 (Actual)
Study Completion Date
July 1, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Imperial College London

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of the study is to assess the accuracy of the Dexcom G6 CGM system and the Abbott FreeStyle Libre flash system compared to the reference standard YSI (Yellow Spring Instruments) glucose in people with diabetes undergoing haemodialysis. The Dexcom G6 is a continuous glucose monitoring system that gives blood glucose values in real-time and includes alarms if the glucose is very low or high. The Abbott FreeStyle ibre flash system is an intermittent glucose monitor that shows the blood glucose values when it is waved near the sensor and does not include alarms. The YSI glucose analysis will take place as a normal part of haemodialysis, by testing blood glucose levels during the haemodialysis session. The study will last 28 days per participant
Detailed Description
Diabetic nephropathy is the leading cause of end-stage renal failure (ESRF), representing approximately 40% of people requiring long-term renal replacement therapy and maintenance haemodialysis [1]. Mortality and morbidity within this cohort is high, with the predominant cause being cardiovascular disease (CVD) [2]. Glycaemic control in many haemodialysis dependent patients with diabetes is poor and may lead to additional renal complications, including high interdialytic weight gain, electrolyte imbalance, and amputations [3]. Current clinical guidance is centred around the prevention of hyperglycaemia and microvascular complications of diabetes. Glucose self-management is particularly challenging due to cyclical changes in insulin sensitivity and circulating insulin concentrations. Hypoglycemia is common due to impaired renal gluconeogenesis, malnutrition, and the increased half-life of insulin and hypoglycemic agents [4, 5]. Additionally, people with chronic kidney disease and diabetes may have other diabetes complications such as retinopathy, neuropathy, and impaired awareness of hypoglycaemia, which can make self-management more difficult. Overall assessment of glycaemic control is also more complex as classical markers of glycemic control (i.e. HbA1c and fructosamine) may be misleading due to the variable underestimation of glycaemia resulting from analytical interferences, shortened half-life of red blood cells and abnormal albumin level [6-8]. Further limitations of HbA1c is that it is not informative regarding glycemic control on the days on and off dialysis, and intra-day glycaemic variability. Frequent capillary blood glucose tests or self-monitoring of blood glucose (SMBG) is the traditional and one of the most effective ways to track an individuals' blood glucose levels. Real-time continuous glucose monitoring (CGM) has been shown to improve overall glucose control, reduce hypoglycaemia in people with an HbA1c <7.0%, and may reduce severe hypoglycaemia [9-11]. In addition, they provide alert and alarm features for hypo- and hyperglycaemia, and for times of rapid glucose change. Flash glucose monitoring does not provide real-time data with alerts and alarms, but allows users to retrospectively review the preceding 8 hours of continuous glucose data, along with a contemporary estimated blood glucose value and trend line. The system consists of a subcutaneous sensor placed on the back of the upper arm, which measures glucose in the interstitial fluid every minute. The glucose data are made available when the user chooses to swipe the reader over the sensor. CGM has the potential to reduce HbA1c and minimize exposure to hypoglycaemia while addressing diabetes distress. Flash glucose monitoring may reduce exposure to hypoglycaemia in people with insulin-treated diabetes. The accuracy of CGM and flash in people with diabetes on haemodialysis has not been described. In this clinical study, the investigators will assess the accuracy of the Dexcom G6 CGM system and the Abbott FreeStyle Libre flash system compared to YSI (Yellow Spring Instruments) glucose in people undergoing haemodialysis.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetic Nephropathies, Type 1 Diabetes Mellitus, Chronic Kidney Diseases
Keywords
Type 1 Diabetes Mellitus, Chronic Kidney Diseases

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Masking Description
Blinded CGM but not Libre
Allocation
N/A
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Dexcom G6 and Abbott Freestyle Libre
Arm Type
Experimental
Arm Description
Participants will have a Dexcom G6 sensor and Abbott FreeStyle Libre sensor inserted in the abdomen and upper arm respectively. Participants will be asked to swipe the FreeStyle Libre reader across the sensor a minimum of every 8 hours. Participants will be asked to continue their usual regimen of self-monitoring capillary blood glucose (SMBG). During haemodialysis, a dialysis circuit blood sample will be drawn at 0 (pre-dialysis) 30, 60, 90, 120, 150, 180, 210 and 240 minutes and immediately after dialysis. Samples from the circuit will be analysed on the YSI glucose analyser. Participants will be asked to change the FreeStyle Libre sensors at day 14. The blinded CGM data will be uploaded at the time of each sensor change by the research team.
Intervention Type
Device
Intervention Name(s)
Dexcom G6 and Abbott Freestyle Libre
Intervention Description
Dexcom G6 - continuous glucose monitoring device - blinded. CE mark 2018 Abbott Freestyle Libre - flash glucose monitoring device. CE mark 2014
Primary Outcome Measure Information:
Title
MARD between G6 and YSI
Description
Mean absolute relative difference between Dexcom G6 and YSI glucose during haemodialysis
Time Frame
28 days
Title
MARD between Libre and YSI
Description
Mean absolute relative difference between Dexcom G6 and YSI glucose during haemodialysis
Time Frame
28 days
Secondary Outcome Measure Information:
Title
HbA1c
Description
Glycated Haemoglobin
Time Frame
28 days
Title
MARD for G6 and YSI <3.9mmol/L
Description
Mean absolute relative difference between Dexcom G6 and YSI glucose <3.9mmol/L
Time Frame
28 days
Title
MARD for Libre and YSI <3.9mmol/L
Description
Mean absolute relative difference between Libre and YSI glucose <3.9mmol/L
Time Frame
28 days
Title
MARD for Libre and YSI 3.9-10mmol/L
Description
Mean absolute relative difference between Libre and YSI glucose 3.9-10mmol/L
Time Frame
28 days
Title
MARD for Libre and YSI >10mmol/L
Description
Mean absolute relative difference between Libre and YSI glucose >10mmol/L
Time Frame
28 days
Title
MARD for G6 and YSI 3.9-10mmol/L
Description
Mean absolute relative difference between Dexcom G6 and YSI glucose 3.9-10mmol/L
Time Frame
28 days
Title
MARD for G6 and YSI >10mmol/L
Description
Mean absolute relative difference between Dexcom G6 and YSI glucose >10mmol/L
Time Frame
28 days
Title
MARD for G6 and YSI 24hr pre
Description
Mean absolute relative difference between Dexcom G6 and YSI glucose during 24 hours prior to heamodialysis
Time Frame
24 hours
Title
MARD for Libre and YSI 24hr pre
Description
Mean absolute relative difference between Libre and YSI glucose during 24 hours prior to heamodialysis
Time Frame
24 hours
Title
MARD for Libre and YSI 24hr post
Description
Mean absolute relative difference between Libre and YSI glucose during 24 hours after heamodialysis
Time Frame
24 hours
Title
MARD for G6 and YSI 24hr post
Description
Mean absolute relative difference between Dexcom G6 and YSI glucose during 24 hours after heamodialysis
Time Frame
24 hours
Title
CEG analysis G6 and YSI
Description
Clarke Error Grid analysis between Dexcom G6 and YSI glucose during haemodialysis
Time Frame
28 DAYS
Title
CEG analysis Libre and YSI
Description
Clarke Error Grid analysis between Libre and YSI glucose during haemodialysis
Time Frame
28 DAYS
Title
Severe hypoglycaemia
Description
Episodes of severe hypoglycaemia
Time Frame
28 days
Title
DKA
Description
Diabetic Ketoacidosis
Time Frame
28 days
Title
Sensor failure
Description
Events of G6/libre sensor failure
Time Frame
28 days
Title
Missing glucose data
Description
Missing blood glucose data for G6/libre measured by number of missing data points
Time Frame
28 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adults >18 years of age Diabetes, with insulin treatment for over 6 months or on sulphonylureas Chronic kidney disease requiring haemodialysis three times per week Exclusion Criteria: Pregnant or planning pregnancy Breastfeeding Enrolled in other clinical trials Have active malignancy or under investigation for malignancy Severe visual impairment Reduced manual dexterity Unable to participate due to other factors, as assessed by the Chief Investigators
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nick Oliver
Organizational Affiliation
Imperial College London
Official's Role
Principal Investigator
Facility Information:
Facility Name
Imperial College London/NHS trust Renal Unit
City
London
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
17986697
Citation
Coresh J, Selvin E, Stevens LA, Manzi J, Kusek JW, Eggers P, Van Lente F, Levey AS. Prevalence of chronic kidney disease in the United States. JAMA. 2007 Nov 7;298(17):2038-47. doi: 10.1001/jama.298.17.2038.
Results Reference
background
PubMed Identifier
12641872
Citation
Levin A. Clinical epidemiology of cardiovascular disease in chronic kidney disease prior to dialysis. Semin Dial. 2003 Mar-Apr;16(2):101-5. doi: 10.1046/j.1525-139x.2003.16025.x.
Results Reference
background
PubMed Identifier
26457201
Citation
Creme D, McCafferty K. Glycaemic Control Impact on Renal Endpoints in Diabetic Patients on Haemodialysis. Int J Nephrol. 2015;2015:523521. doi: 10.1155/2015/523521. Epub 2015 Sep 20.
Results Reference
background
PubMed Identifier
23067652
Citation
National Kidney Foundation. KDOQI Clinical Practice Guideline for Diabetes and CKD: 2012 Update. Am J Kidney Dis. 2012 Nov;60(5):850-86. doi: 10.1053/j.ajkd.2012.07.005. Erratum In: Am J Kidney Dis. 2013 Jun;61(6):1049.
Results Reference
background
PubMed Identifier
10803766
Citation
Haviv YS, Sharkia M, Safadi R. Hypoglycemia in patients with renal failure. Ren Fail. 2000 Mar;22(2):219-23. doi: 10.1081/jdi-100100866.
Results Reference
background
PubMed Identifier
12043937
Citation
Lee KF, Szeto YT, Benzie IF. Glycohaemoglobin measurement: methodological differences in relation to interference by urea. Acta Diabetol. 2002 Apr;39(1):35-9. doi: 10.1007/s005920200010.
Results Reference
background
PubMed Identifier
17267743
Citation
Inaba M, Okuno S, Kumeda Y, Yamada S, Imanishi Y, Tabata T, Okamura M, Okada S, Yamakawa T, Ishimura E, Nishizawa Y; Osaka CKD Expert Research Group. Glycated albumin is a better glycemic indicator than glycated hemoglobin values in hemodialysis patients with diabetes: effect of anemia and erythropoietin injection. J Am Soc Nephrol. 2007 Mar;18(3):896-903. doi: 10.1681/ASN.2006070772. Epub 2007 Jan 31.
Results Reference
background
PubMed Identifier
11840370
Citation
Joy MS, Cefalu WT, Hogan SL, Nachman PH. Long-term glycemic control measurements in diabetic patients receiving hemodialysis. Am J Kidney Dis. 2002 Feb;39(2):297-307. doi: 10.1053/ajkd.2002.30549.
Results Reference
background
PubMed Identifier
21737469
Citation
Pickup JC, Freeman SC, Sutton AJ. Glycaemic control in type 1 diabetes during real time continuous glucose monitoring compared with self monitoring of blood glucose: meta-analysis of randomised controlled trials using individual patient data. BMJ. 2011 Jul 7;343:d3805. doi: 10.1136/bmj.d3805.
Results Reference
background
PubMed Identifier
28118453
Citation
Beck RW, Riddlesworth T, Ruedy K, Ahmann A, Bergenstal R, Haller S, Kollman C, Kruger D, McGill JB, Polonsky W, Toschi E, Wolpert H, Price D; DIAMOND Study Group. Effect of Continuous Glucose Monitoring on Glycemic Control in Adults With Type 1 Diabetes Using Insulin Injections: The DIAMOND Randomized Clinical Trial. JAMA. 2017 Jan 24;317(4):371-378. doi: 10.1001/jama.2016.19975.
Results Reference
background
PubMed Identifier
28118454
Citation
Lind M, Polonsky W, Hirsch IB, Heise T, Bolinder J, Dahlqvist S, Schwarz E, Olafsdottir AF, Frid A, Wedel H, Ahlen E, Nystrom T, Hellman J. Continuous Glucose Monitoring vs Conventional Therapy for Glycemic Control in Adults With Type 1 Diabetes Treated With Multiple Daily Insulin Injections: The GOLD Randomized Clinical Trial. JAMA. 2017 Jan 24;317(4):379-387. doi: 10.1001/jama.2016.19976. Erratum In: JAMA. 2017 May 9;317(18):1912.
Results Reference
background

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Assessment of the Accuracy of Continuous Glucose Sensors in People With Diabetes Undergoing Haemodialysis

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