Tailored diet shows promise for diabetes control
NCT ID NCT07472855
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a personalized dietary program for 30 adults with type 2 diabetes. The program was designed to help participants better manage their blood sugar and potentially achieve remission. Researchers measured changes in HbA1c and other health markers to see if the diet approach was feasible and effective.
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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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30 people
The number who actually took part.
- Started
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Jun 2025
- Finished
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Dec 2025
- 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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Children (under 18), adults (18 to 64) and older adults (65 and over)
- 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: * Meet 1999 WHO diagnostic criteria for type 2 diabetes mellitus (diabetes symptoms plus random plasma glucose ≥11.1 mmol/L, or fasting plasma glucose ≥7.0 mmol/L, or 2-hour plasma glucose ≥11.1 mmol/L after OGTT) Glycated hemoglobin (HbA1c) between 7% and 10%; * Stable glucose-lowering medication regimen as assessed by physician; * Age 18-60 years; * Light physical labor in the past 6 months (work mainly involving standing or small amount of walking); * Willing to participate voluntarily, understand study content, and able to attend regular follow-up; Exclusion Criteria: * Currently using weight-loss medications; * Significant renal insufficiency (creatinine ≥1.5 mg/dL or 133 μmol/L); * Significant liver dysfunction (ALT more than 2 times the upper limit of normal); * History of stroke or myocardial infarction; * Other serious diseases including malignant tumors, psychiatric disorders, anorexia, or gastrointestinal diseases; * Pregnancy, planning pregnancy, postpartum status, or breastfeeding;
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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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Beijing Luhe Hospital, Capital Medical University
Beijing, China
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