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Can a smart carb diet tame type 2 diabetes?
NCT ID NCT06936657
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study will test whether a diet with carefully chosen carbohydrates can improve blood sugar control in people with type 2 diabetes. 150 adults will try both an optimized carbohydrate diet and a standard diabetes diet for 12 weeks each, with a break in between. The goal is to see if the special diet leads to better glucose levels and other health benefits.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- optimized carbohydrate diet
- What this could lead to
- If successful, this diet could offer a better way to manage blood sugar and improve overall health in people with type 2 diabetes.
- What could go wrong
- This is a dietary intervention study, not a drug trial. Results may vary, and the diet requires strict adherence. It is not yet recruiting, so outcomes are uncertain.
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 150 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Oct 2025
An estimate. Start dates often move.
- Expected to finish
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Oct 2027
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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35 to 70 years
- 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.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Patients diagnosed with type 2 diabetes according to the ADA diagnostic criteria 2. HbA1c ≥ 7% and \< 9% 3. Antidiabetic medication has been stable for at least 3 months before recruitment 4. Aged 35-70 years 5. Signed the informed consent form Exclusion Criteria: 1. Treatment with insulin 2. Treatment with GLP-1 receptor agonists or DPP-4 inhibitors 3. Occurrence of diabetic ketoacidosis, lactic acidosis, hyperosmolar coma, or recurrent severe hypoglycemia within the past year 4. Having one or more severe chronic diabetic complications, including advanced diabetic retinopathy, macroalbuminuria (urine albumin-to-creatinine ratio ≥300 mg/g), or impaired renal function (eGFR ≤60 ml/min/1.73 m²) 5. Presence of cardiovascular events (e.g., myocardial infarction, stent placement, unstable angina, heart failure, cardiac dysfunction) or cerebrovascular diseases (e.g., intracerebral hemorrhage, ischemic stroke) within the past 6 months 6. Diagnosis of acute or chronic gastrointestinal diseases (e.g., ulcers), hyperthyroidism or hypothyroidism, uncontrolled hypertension, active malignancy not in remission, or other life-threatening diseases 7. Recent use of antibiotics, probiotics, or prebiotics within the past 3 weeks or need for long-term use 8. Unstable medication regimen or use of prescription medications affecting metabolism (e.g., thyroid hormones, glucocorticoids) 9. Pregnancy, breastfeeding, or planning pregnancy 10. Presence of a pacemaker or metal implants, claustrophobia, or other contraindications to fMRI 11. Psychiatric disorders impairing cooperation 12. Expected poor compliance 13. Current or recent (within 4 weeks prior to study initiation) participation in other clinical trials
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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 official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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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.
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