DysglycemiaEUGLYCARENCT07263789
Effect of a Food Supplement on Blood Glucose Levels in Patients With Impaired Glucose Values
A study testing Nutraceutical supplements in people with Dysglycemia, run by Fondazione IRCCS Policlinico San Matteo di Pavia at 2 sites in Italy.
Trial summary
The primary objective is to evaluate the efficacy of Euglycem® plus recommended standard diet on reducing FPG compared to baseline and to recommended standard diet alone after 3 months Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Dysglycemia
- What is being tested?
- Nutraceutical supplements
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 108 participants
- Where
- 2 sitesItaly
- Study dates
- 8 Apr 2025to 31 Jan 2026
- Phase
- Interventional
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- BMI ≤30 kg/m2
- subjects able to understand the informed consent and sign it before enrollment in the study
- subjects willing to follow all study requirements and perform all study visits as well as collaborate with the investigator.
Who cannot join
- ongoing treatment with drugs that can affect blood glucose
- current participation in another investigational drug or investigational device trial or inclusion in another investigational drug or investigational device trial within the previous month
Trial locations and contacts
2 sites in 1 country. Contact the study team or a site near you to ask about taking part.
Italy2 sites, 2 recruiting
- Recruiting
IRCCS Policlinico San Matteo
Pavia, Lombardy, 27100
Giuseppe Derosa, MD, +390382502614, g.derosa@smatteo.pv.it
- Not yet recruiting
Fondazione IRCCS Policlinico San Matteo di Pavia
Pavia, Pavia, 27100
Giuseppe Derosa, G.Derosa@smatteo.pv.it
About this study
Official title: Randomized, Open-label, Parallel Group Study to Evaluate the Efficacy of Euglycem in Reducing Blood Glucose in Patients With Dysglycemia After Three Months of Treatment - EUGLYCARE Study
The primary objective is to evaluate the efficacy of Euglycem® plus recommended standard diet on reducing FPG compared to baseline and to recommended standard diet alone after 3 months
Read the detailed description
Dysglycemia (or prediabetes) is a reversible metabolic condition that increases the risk of developing type 2 diabetes mellitus, a pathological condition that, in prognostic terms, is considered equivalent to cardiovascular disease. Type 2 diabetes mellitus, therefore, is a serious pathology not only for the symptoms and complications related to it but also for the prognosis. Dysglycemia is characterized by an alteration in blood glucose levels that do not yet fall within the diagnostic criteria for diabetes. It is a very common condition that often remains unknown because it is asymptomatic. Dysglycemia is due to a receptor dysregulation between cellular and circulating glucose values and pancreatic insulin production, characterized by an initial resistance to insulin produced by pancreatic beta cells and directed to the muscle cells. Insulin acts as a catalyst for the use of glucose for metabolic purposes with consequent withdrawal of circulating glucose and, therefore, reduction of glycemia. If this regulation does not work perfectly, blood glucose levels increase and the condition of dysglycemia is feared. The main risk factors associated with dysglycemia are overweight and obesity, family history of diabetes, sedentary lifestyle, hypertension and hypercholesterolemia, all risk factors also for cardiovascular diseases. In women dysglycemia is often also correlated with polycystic ovary and gestational diabetes. There is evidence that dysglycemia and type 2 diabetes are associated with a deficiency of vitamin D. The pancreatic beta cells, responsible for the release of insulin, express receptors for vitamin D and their dysfunction is demonstrated in various experimental models. However, the administration of vitamin D to subjects with dysglycemia or diabetes has produced uncertain results. Dysglycemia is a silent condition, therefore asymptomatic, although subjects with dysglycemia are, in general, already exposed to an increased risk of developing cardiovascular diseases. Consequentially, the diagnosis is exclusively laboratory, i.e. a fasting blood glucose (FPG) between 100 and 125 mg/dl, a glucose load curve (OGTT) whose result after two hours is higher than 140 mg/dl (normal limit) and less than 200 mg/dl (diagnostic criterion for type 2 diabetes mellitus), i.e. between 140-199 mg/dl and glycated hemoglobin (HbA1c) values between 5.7-6.4%. It is believed that approximately 11% of subjects with dysglycemia develop type 2 diabetes after three years. This percentage rises to 25% after five years. The remedies to overcome the prediabetic condition are essentially based on the reduction of risk factors and relative improvement of lifestyle. A healthy diet, low in fat and rich in fiber and vegetable protein is important together with physical activity to be practiced according to World Health Organization (WHO) recommendations. To date, no drug is approved for the treatment of dysglycemia, while substances of natural origin have been shown to contribute to the normalization of glucose metabolism in association with the above mentioned remedies which are known to present long-term compliance problems. This is the context in which the association of banaba leaves extract and chromium picolinate (Euglycem®) is positioned. Chromium is an essential mineral that improves insulin sensitivity. It also has favorable effects on the metabolism of proteins, carbohydrates and fats and leads to a reduction in body weight. Chromium deficiency is rare, but significant, because it results in poorer glycemia and cholesterolemia control. Banaba leaves extract promotes the absorption of glucose and its use for energy purposes, thus playing a role in the regulation of blood glucose and insulin levels. By regulating glycemia fluctuations that activate the hunger center, banaba is useful for reducing body weight and triglyceride levels. One study reported that in 10 healthy subjects who received 1 tablet/day of Euglycem containing 50 mg of banaba leaves extract or placebo for 4 days, the supplement significantly reduced the glucose area under the curve (AUC) and insulinemia after glucose load compared to placebo. The same study also evaluated the effect of the supplement in 40 subjects with dysglycemia randomized to receive 1 tablet/day of Euglycem containing 10 mg or 50 mg of banaba leaves extract for 4 weeks associated with an improvement in dietary and behavioral habits. It was highlighted that both dosages improved weight, body mass index (BMI), FPG and Homeostasis Model Assessment (HOMA) index compared to baseline while only the highest dose significantly reduced fasting plasma insulin (FPI) and HbA1c compared to baseline. However, the study has important limitations such as the small number of subjects enrolled and the short duration of treatment.
- Conditions
- Dysglycemia
- Being tested
- Nutraceutical supplements, Placebo
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Nutraceutical supplementsDietary supplement
An association of banaba leaves extract and chromium picolinate (Euglycem®) will be administered
PlaceboDietary supplement
Placebo
| Study group | Role | What they receive |
|---|---|---|
| Euglycem | Active comparator | An association of banaba leaves extract and chromium picolinate Receives: Dietary Supplement: Nutraceutical supplements |
| Placebo | Placebo comparator | Placebo Receives: Dietary Supplement: Placebo |
What is being measured
The primary outcome is the main question the study is designed to answer.
Dysglicemia
The primary objective is to evaluate the efficacy of Euglycem® plus recommended standard diet on reducing FPG compared to baseline and to recommended standard diet alone after 3 months of supplementation.
Measured: 3 months
Secondary outcomes (3)
Insulin reistance
The secondary objective is to evaluate the efficacy of Euglycem® plus recommended standard diet on reducing HbA1c, FPI and HOMA index
Measured: 3 months
Vitamin D3 levels
The secondary objective is to evaluate the efficacy of Euglycem® plus recommended standard diet on the variation of vitamin D3 levels
Measured: 3 months
Glycemic status
The secondary objective is to evaluate the efficacy of Euglycem® plus recommended standard diet on the proportion of subjects pass from impaired fasting glycemia (IFG) condition to euglycemia and the proportion of subjects pass from impaired glucose tolerance (IGT) condition to euglycemia
Measured: 3 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted4 Dec 2025
- Study start8 Apr 2025
- Primary completion31 Dec 2025 (estimated)
- Study completion31 Jan 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for DysglycemiaStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind
- Who is masked
- Participant, Investigator
- Enrolment
- 108 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Fondazione IRCCS Policlinico San Matteo di Pavia
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Giuseppe Derosa, Fondazione IRCCS Policlinico San Matteo di Pavia
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07263789
- Sponsor's protocol ID
- EUGLYCARE
- Acronym
- EUGLYCARE
- Status last verified
- Nov 2025
- First submitted
- 23 Nov 2025
- Last updated
- 4 Dec 2025
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No