Can a smart sensor beat finger sticks for diabetes control?
NCT ID NCT05944432
First seen Jun 27, 2026 · Last updated Aug 21, 2026 · Updated 1 time
Summary
This study compares continuous glucose monitoring using the FreeStyle Libre 3 sensor to standard finger-stick testing in 470 adults with type 2 diabetes whose blood sugar is not well controlled. Participants continue their usual medications (basal insulin plus SGLT2 inhibitor and/or GLP-1). The main goal is to see if the sensor improves HbA1c levels over 16 weeks. This is a management study, not a cure, as diabetes requires ongoing care.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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469 people
The number who actually took part.
- Started
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Jul 2023
- Expected to finish
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Nov 2027
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Aged 18 years or over. * Type 2 diabetes diagnosis for ≥1 year prior to enrolment. * Type 2 diabetes treated with a basal insulin injection regimen and SGLT2 inhibitor and/or GLP-1. * Screening HbA1c ≥59 mmol/mol to ≤97 mmol/mol (≥7.5% and ≤11.0%, inclusive). Exclusion Criteria: * Participant is currently prescribed prandial or pre-mixed (biphasic) insulin at enrolment. * Currently participating in another study that could affect glucose measurements or glucose management. * A female participant who is pregnant. * A breastfeeding female participant. * Bariatric surgical procedure within the past 12 months or is planning/scheduled for bariatric surgery within the study duration.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Cambridge University Hospital (Addenbrookes)
Cambridge, United Kingdom
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Churchill Hospital
Oxford, United Kingdom
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Darlington Memorial Hospital
Darlington, United Kingdom
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Derriford Hospital
Plymouth, United Kingdom
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Hull Royal Infirmary
Hull, United Kingdom
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Ipswich Hospital
Ipswich, United Kingdom
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King's College Hospital
London, United Kingdom
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Leicester General Hospital
Leicester, United Kingdom
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Manchester Royal Infirmary
Manchester, M13 9WU, United Kingdom
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Moorgreen Hospital
Southampton, United Kingdom
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Ninewells Hospital
Dundee, United Kingdom
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Norfolk and Norwich University Hospital
Norwich, United Kingdom
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Northern General Hospital
Sheffield, United Kingdom
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Northwick Park Hospital
Harrow, United Kingdom
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Princess Alexandra Hospital
Harlow, United Kingdom
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Queen Alexandra Hospital
Portsmouth, United Kingdom
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Queen Elizabeth Hospital
Birmingham, United Kingdom
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Royal Derby Hospital
Derby, DE22 3NE, United Kingdom
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Royal United Hospital
Bath, United Kingdom
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Singleton Hospital
Swansea, United Kingdom
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St James University Hospital
Leeds, United Kingdom
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St Mary's Hospital
London, United Kingdom
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Tameside General Hospital
Ashton-under-Lyne, United Kingdom
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The Adam Practice
Poole, United Kingdom
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Wishaw Hospital
Wishaw, United Kingdom
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Other studies related to the condition(s) this trial covers.
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