Evaluating Safe Ketone Thresholds To Minimise Ketosis in People With Type 1 Diabetes Using Dapagliflozin

Trial statusNot yet recruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age24-85
SponsorSt Vincent's Hospital Melbourne

About this trial

Sodium glucose cotransporter 2 (SGLT2) inhibitors are a type of medicine that help the kidneys get rid of extra sugar in the blood through urine. In people with type 2 diabetes (T2D), these medications help lower blood sugar levels, help people lose weight and improve heart and kidney health.

SGLT2 inhibitors are mainly used in T2D, however some studies show they might also help people with type 1 diabetes (T1D). The same health benefits observed in people with T2D the investigators anticipate may help those with T1D. Currently, there is a safety concern that people with T1D using these medicines can raise the risk of diabetic ketoacidosis (DKA). DKA occurs when the body doesn't have enough insulin (a hormone made in the pancreas that helps your body use sugar (glucose) for energy), it starts to break down fats as a source of energy. This breakdown of fats produces ketones. Very high levels of ketones in the blood can make the blood acidic (toxic) and lead to DKA. If not treated in time, this can make the person living with T1D very ill and can be life-threatening. Because of this risk, health agencies like the FDA in the U.S., and the TGA in Australia have not approved use of SGLT2 inhibitors for people with T1D.

Still, some experts believe SGLT2 inhibitors may safely be used alongside insulin in T1D if DKA risk is carefully managed. This might be possible with early detection and treatment of rising ketone levels. One approach is using continuous ketone monitors, which track ketone levels in real time and can alert users early. People would also need proper education on what to do if ketone levels start rising.

To date, there's no official agreement on the exact ketone level that should trigger action. Some suggest action when ketone levels reach 1.0 or 1.5 mmol/L. A lower limit like 1.0 mmol/L may be safer, but it could also lead to too many alarms and extra stress, or unnecessary eating to bring ketones down.

Therefore, the aim of this study is to assess if initiating responses to elevated ketone levels at a threshold of 1.0 mmol/L, compared to a threshold of 1.5 mmol/L, will reduce the risk of DKA in people with T1D using Dapagliflozin.

The investigators will recruit 115 adults with T1D and provide Dapagliflozin (SGLT2 inhibitor) and continuous glucose and ketone monitoring (DGK) devices. Participants will be randomly assigned to two groups. Group 1 will wear a DGK with alarms set at ketone level of 1.0 mmol/L and receive education about taking action when ketone levels are ≥1.0 mmol/L. Group 2 will wear a DGK with alarms set at ketone level of 1.5 mmol/L and receive education about taking action when ketone levels are ≥1.5 mmol/L. Participants will be assessed for time spent with critically high ketone levels, incidence of DKA, glucose and person reported outcomes.

Findings from this study will provide real life data and clinical evidence to help guide safe use of SGLT2 inhibitors in people with T1D by informing protocols for monitoring and managing associated DKA risks.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Aged between 24 and 85 years of age inclusive (66% 24Y to 65Y; and 33% >65Y to 85Y)

Diagnosed with T1D (made on clinical criteria) for at least 1 year

Insulin regimen either on MDI or insulin pump with at least 40% in one mode

Minimum total daily insulin dose 0.4 Units per kg / day (can be on insulin pump or MDI);

Disqualifiers

Pregnancy or planned pregnancy

eGFR <30ml/min/1.73m2

History of DKA in the last 12 months

Use of low carbohydrate diet (<100g/day)

Trial design

Design model

Parallel

Treatments tested in this trial

  • FORXIGA

    Drug

    All participants will take FORXIGA (Dapagliflozin) orally at a dose of 10mg/day for 12 weeks

Treatment groups

115 Participants
are divided into 2 treatment groups
Group A: Dual glucose and ketone (DGK) sensor threshold 1.0mmol/LActive comparator 1 intervention
Group B: Dual glucose and ketone (DGK) sensor threshold 1.5mmol/LActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Percent time spent with interstitial ketones ≥3.0mmol/L (Main Study)

Percent of time spent with interstitial ketone levels ≥3.0mmol/L on dual glucose / ketone monitoring device during 12-weeks of taking Dapagliflozin

Time frame
Commencement to end of study (12 weeks)
2

Percent of time spent with interstitial ketones ≥3.0mmol/L during exercise (Exercise Study)

Percent of time spent with interstitial ketones ≥3.0mmol/L on dual glucose / ketone monitoring device from start of exercise to 12 hours post-commencement of exercise

Time frame
Weeks 4 to12

Secondary outcomes

1

Percent of time with ketone levels in different ranges

Percent time with interstitial ketone levels of: 1. \>0.6 mmol/L 2. \>1.0 mmol/L 3. \>1.5mmol/L

Time frame
Commencement to end of study (12 weeks)
2

Mean interstitial ketone levels

Average if ketone levels measured by dual glucose / ketone monitor device over 12 weeks

Time frame
Commencement to end of study (12 weeks)
3

Incidence of diabetic ketoacidosis (DKA)

Number of DKA events

Time frame
Commencement to end of study (12 weeks)
4

Change in HbA1c

Difference in HbA1c (mmol/mol) between baseline and study end

Time frame
Week 0 and Week 12 from study commencement

Other outcomes

1

Percent time of sensor wear

Percentage of time dual glucose/ketone sensor is worn during the 12 weeks of the study

Time frame
Commencement to end of study (12 weeks)
2

Incidence of sensor- related skin infections

Number of skin infections at site of sensor insertion

Time frame
Commencement to end of study (12 weeks)
3

Mean duration of sensor survival before replacement

Number of days dual glucose/ketone sensor is working for before needing replacement

Time frame
Commencement to end of study (12 weeks)
4

Difference between blood and interstitial ketones values

Difference between ketone readings from the dual ketone/glucose sensor (study sensor) and fingerprick blood ketone test (standard of care)

Time frame
Commencement to end of study (12 weeks)

Sponsors and contacts

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St Vincent's Hospital Melbourne

Lead sponsor

Baker Heart and Diabetes Institute

Collaborator

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Collaborator

University of Melbourne

Collaborator

Melbourne Health

Collaborator

Austin Health

Collaborator

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