Could a smart glucose meter transform diabetes care?
NCT ID NCT07774078
First seen Aug 19, 2026 · Last updated Aug 21, 2026 · Updated 2 times
Summary
This trial tests whether remote monitoring can help people with diabetes better control their blood sugar. Participants will either use a connected glucose meter that sends readings to a platform for remote management, or receive standard care. The study will compare changes in blood sugar and HbA1c levels over six months to see if telemonitoring makes a difference.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Telemonitoring with a connected blood glucose meter and mobile/web platform
- What this could lead to
- If effective, this approach could offer a practical way to help people with diabetes manage their blood sugar more effectively from home.
- What could go wrong
- The trial is relatively small and results may not apply to all diabetes patients. Success depends on patients consistently using the technology.
This is an AI summary of the original study and may miss details. Read our disclaimer.
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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About 260 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Aug 2024
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
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: * Diagnosis of diabetes mellitus with HbA1c between 7% and 10%. * Stable antidiabetic treatment for at least 4 weeks prior to enrollment. Exclusion Criteria: * Serum creatinine \>200 µmol/L. * Acute coronary syndrome or stroke. * Dementia. * Pregnancy. * Inability to participate in or comply with the telemonitoring intervention. * Severe diabetic retinopathy.
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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University Hospital Fattouma Bourguiba Monastir
RECRUITINGMonastir, Tunisia
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