Effect of a Food Supplement on Blood Glucose Levels in Patients With Impaired Glucose Values (EUGLYCARE)
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
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Detailed Description
Study Type
Study Type
Enrollment (Estimated)
Enrollment
Phase
Phase
- Not Applicable
Contacts and Locations
Study Contact
Study Contact
- Name: Giuseppe Derosa, MD
- Phone Number: +390382502614
- Email: g.derosa@smatteo.pv.it
Study Locations
-
-
Lombardy
-
Pavia, Lombardy, Italy, 27100
- Recruiting
- IRCCS Policlinico San Matteo
-
Contact:
- Giuseppe Derosa, MD
- Phone Number: +390382502614
- Email: g.derosa@smatteo.pv.it
-
-
Pavia
-
Pavia, Pavia, Italy, 27100
- Not yet recruiting
- Fondazione IRCCS Policlinico San Matteo di Pavia
-
Contact:
- Giuseppe Derosa
- Email: G.Derosa@smatteo.pv.it
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- 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.
Exclusion Criteria:
- 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
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
Placebo Comparator: Placebo
|
Placebo
|
|
Active Comparator: Euglycem
An association of banaba leaves extract and chromium picolinate
|
An association of banaba leaves extract and chromium picolinate (Euglycem®) will be administered
|
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Dysglicemia
Time Frame: 3 months
|
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.
|
3 months
|
Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Insulin reistance
Time Frame: 3 months
|
The secondary objective is to evaluate the efficacy of Euglycem® plus recommended standard diet on reducing HbA1c, FPI and HOMA index
|
3 months
|
|
Vitamin D3 levels
Time Frame: 3 months
|
The secondary objective is to evaluate the efficacy of Euglycem® plus recommended standard diet on the variation of vitamin D3 levels
|
3 months
|
|
Glycemic status
Time Frame: 3 months
|
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
|
3 months
|
Collaborators and Investigators
Sponsor
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Study Start
Primary Completion (Estimated)
Primary Completion
Study Completion (Estimated)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Estimated)
First Posted
Study Record Updates
Last Update Posted (Estimated)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
Other Study ID Numbers
- EUGLYCARE
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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