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Assessment of the Impact of Real-Time Continuous Glucose Monitoring on People Presenting With Severe Hypoglycaemia

Assessment of the Impact of Real-Time Continuous Glucose Monitoring on People Presenting With Severe Hypoglycaemia

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03748433
Acronym
AIR-CGM
Enrollment
35
Registered
2018-11-20
Start date
2019-01-03
Completion date
2021-09-09
Last updated
2024-03-22

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

Conditions

Diabetes Mellitus, Type 1, Hypoglycemia, Hypoglycemia Unawareness

Keywords

Real time continuous glucose monitoring, continuous subcutaneous insulin infusion, self monitoring blood glucose, sensor augmented pump, severe hypoglycaemia, hypounaware

Brief summary

This study aims to assess the impact of real-time continuous glucose monitoring on the frequency, duration, awareness and severity of hypoglycaemia in people with type 1 diabetes and a recent history of severe hypoglycaemia, compared to usual care.

Detailed description

Type 1 diabetes (T1DM), which affects 300,000 in the UK, is characterised by autoimmune destruction of the pancreatic beta cells, leading to absolute deficiency of insulin. Management of T1DM requires exogenous insulin administration, aiming for glucose concentrations as close to physiological values as possible. Intensive management of T1DM improves glucose control and reduces the risk of microvascular diabetes complications and cardiovascular disease1. In the UK diabetes consumes more than 10% of the National Health Service budget 2 and in the USA a relatively greater amount is spent on type 1 compared with type 2 diabetes (8.6% of the diabetes budget compared with 5.6% of diabetes prevalence)3. Medication and insulin pump therapy accounts for less than 10% of diabetes expenditure with the majority of costs incurred in the treatment of complications4. Optimal control remains challenging to achieve and intensive insulin treatment increases the risk of severe hypoglycaemia, with lower glucose values also associated with an increased frequency and severity of moderate hypoglycaemia5, 6. Severe hypoglycaemia is defined as any episode of hypoglycaemia requiring the assistance of a third party actively to treat. Hypoglycaemia is associated with morbidity and even mortality, and places a financial burden on health systems. Severe hypoglycaemia costs £13million per year in NHS costs7. Between 4 and 10% of deaths in people with type 1 diabetes are attributed to hypoglycaemia and the risk of severe hypoglycaemia increases 6-fold in people with impaired awareness of hypoglycaemia. Avoidance of hypoglycaemia is associated with restoration of hypoglycaemia awareness and this may be enabled by the use of continuous glucose monitoring. In type 1 diabetes real-time continuous glucose monitoring (CGM) improves overall glucose control in all age groups when used continuously, reduces hypoglycaemia in people with an HbA1c \<7.0%, and may reduce severe hypoglycaemia8-10. The predictive Low-Glucose suspend (PLGS) feature in sensor augmented insulin pumps (SAP) automatically reduces insulin delivery when trends in CGM glucose concentrations predict future hypoglycaemia, and significantly reduces hypoglycaemia without rebound hyperglycaemia compared to SAP without PLGS11. In England continuous glucose monitoring is supported by NICE for people with type 1 diabetes who are willing to commit to using it at least 70% of the time and to calibrate it as needed, and who have any of the following despite optimised use of insulin therapy and conventional blood glucose monitoring12: * More than 1 episode a year of severe hypoglycaemia with no obvious preventable precipitating cause. * Complete loss of awareness of hypoglycaemia. * Frequent (more than 2 episodes a week) asymptomatic hypoglycaemia that is causing problems with daily activities. * Extreme fear of hypoglycaemia. * Hyperglycaemia (HbA1c level of 75 mmol/mol \[9%\] or higher) that persists despite testing at least 10 times a day Addressing severe hypoglycaemia, reducing the risk of further episodes and acting promptly to optimise hypoglycaemia awareness are critical in people at high risk. Continuous subcutaneous insulin pump therapy is supported for adults and children over 12 with type 1 diabetes in whom attempts to achieve target haemoglobin A1c (HbA1c) with multiple daily injections (MDI) have resulted in disabling hypoglycaemia or HbA1c levels have remained high (8.5% \[69 mmol/mol\] or above) despite high level care12.

Interventions

Commercially available Dexcom G6 Continuous Glucose Monitoring

DEVICETandem t:slim X2 Insulin Pump

sensor augmented insulin pump with predictive low glucose suspend

Sponsors

London Ambulance Service
CollaboratorOTHER
Imperial College London
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Randomised open-label parallel group study

Eligibility

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

Inclusion criteria

PRE-REGISTRATION EVALUATIONS * Episode of severe hypoglycaemia * Age \>18 years * Diagnosis of type 1 diabetes INCLUSION CRITERIA * Adults over 18 years of age * Severe hypoglycaemia requiring ambulance call-out or emergency department attendance within 2 weeks * Type 1 diabetes confirmed on the basis of clinical features * Type 1 diabetes for greater than 3 years

Exclusion criteria

* Use of CGM within the last 6 months (except short periods of diagnostic blinded use under clinic supervision). Prior use of Abbott FreeStyle Libre Device is permitted. * Use of pre-mixed insulin * No access to smartphone or computer * Pregnant or planning pregnancy * Breastfeeding * 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 WITHDRAWAL CRITERIA Participants will be withdrawn if their ability to give informed consent is impaired. Participants will also be withdrawn, at the chief investigators discretion, if glucose control is negatively impacted by the use of either intervention.

Design outcomes

Primary

MeasureTime frameDescription
Time Spent in Hypoglycaemia12 weeksPercentage time spent in hypoglycaemia (\<3.0mmol/L, 55mg/dL)

Countries

United Kingdom

Participant flow

Recruitment details

Recruitment was undertaken in collaboration with the London Ambulance Service. Participants were identified following an episode of severe hypoglycaemia. Following any questions, London Ambulance Services and Emergency Departments obtained verbal consent to share details with study investigators, and sent details to principal investigator through a secure website (NHS.net account). Prrticipants had to be enrolled within two weeks of the severehypoglycaemia episode.

Pre-assignment details

Once participants were enrolled they were randomised to either real-time CGM (intervention) or self-monitoring of blood glucose (standard care) for 12 weeks.

Participants by arm

ArmCount
Continuous Glucose Monitoring (CGM)
The RT CGM group will receive a Dexcom G6 transmitter and sensors, as well as a structured education refresher focusing on hypoglycaemia avoidance, recognition, and management. Dexcom G6 CGM: Commercially available Dexcom G6 Continuous Glucose Monitoring
16
Self Monitoring Blood Glucose (SMBG)
The SMBG group will additionally undergo blinded CGM at weeks 1 and 2, weeks 4 to 6 and weeks 9 to 12 using the Dexcom G6 system. Participants in this group will be shown how to insert the Dexcom G6 at the first clinic visit and sensors provided so they can do this at home.
14
Total30

Baseline characteristics

CharacteristicContinuous Glucose Monitoring (CGM)TotalSelf Monitoring Blood Glucose (SMBG)
Age, Continuous38.5 years41 years45.5 years
Ethnicity (NIH/OMB)
Hispanic or Latino
0 Participants0 Participants0 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
0 Participants0 Participants0 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
16 Participants30 Participants14 Participants
Region of Enrollment
United Kingdom
16 participants30 participants14 participants
Sex: Female, Male
Female
8 Participants13 Participants5 Participants
Sex: Female, Male
Male
8 Participants17 Participants9 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 160 / 14
other
Total, other adverse events
0 / 160 / 14
serious
Total, serious adverse events
0 / 164 / 14

Outcome results

Primary

Time Spent in Hypoglycaemia

Percentage time spent in hypoglycaemia (\<3.0mmol/L, 55mg/dL)

Time frame: 12 weeks

Population: Participants who had sufficient data were included in analysis of primary outcome

ArmMeasureValue (MEDIAN)
Continuous Glucose Monitoring (CGM)Time Spent in Hypoglycaemia1.8 percentage time
Self Monitoring Blood Glucose (SMBG)Time Spent in Hypoglycaemia3.3 percentage time

Source: ClinicalTrials.gov · Data processed: Mar 1, 2026