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China Probiotics Premix for Blood Glucose Management - Top Suppliers & Factory-Backed Clinical Strains

Deposite: CCTCC M 2020833

Shelf life: 24 months

Storage conditions: Stored at -18℃or lower

Health Benefits
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Discover cutting-edge clinical research from leading hospitals in China that focuses on activating the pancreas and effectively regulating blood sugar and blood lipids. Our product is sourced from trusted suppliers and manufactured in our state-of-the-art factory, ensuring the highest quality and efficacy for your health needs.

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    🧬 Functional Strains

    Bifidobacterium animalis subsp. lactis F1-7
    Bifidobacterium animalis subsp. lactis BA-C9
    Lactiplantibacillus plantarum YZX21
    Lactiplantibacillus plantarum F3-2
    Lactiplantibacillus plantarum H-87
    Lacticaseibacillus paracasei G15

    🎯 Main Functions

    Lower blood glucose
    Reduce body weight
    Adjuvant therapy

    📊 Clinical Studies & Patents

    ✨ 1 Clinical Study
    💡 6 Invention Patents
    📚 17 Literature Studies
    Clinical Registration Number: ChiCTR2400089551—A Randomized, Double-Blind, Placebo-Controlled Feeding Trial of Compound Lactic Acid Bacteria Powder for Improving Blood Glucose, Blood Lipids, and Body Mass Index in Patients with Type 2 Diabetes.
    • Achieved HbA1c <7.0 % within 90 days.
    • Improved insulin resistance, with a significant reduction in HOMA-IR.
    • Average weight reduction of 3.66 kg, with an average BMI decrease of 1.41.
    Invention Patent: ZL202110019976.3 - A method for preparing and applying a combination of Bifidobacterium animalis subsp. lactis F1-7 and krill oil to improve atherosclerosis inflammation.

    🏥 Tertiary Hospital · Clinical Evidence-Based Medicine

    A Randomized, Double-Blind, Placebo-Controlled Feeding Trial of SugaRite ™ Premix Probiotics Powder for Improving Blood Glucose, Blood Lipids, and Body Mass Index in Patients with Type 2 Diabetes.
    Research Institution
    The Second Affiliated Hospital of Zhejiang University School of Medicine (a Grade III, Level A general hospital)
    Total Sample Size
    60 patients with Type 2 Diabetes
    Intervention Duration
    90 consecutive days of trial consumption
    Intervention Protocol
    2g, twice daily
    Primary Efficacy Endpoints
    HbA1c, blood glucose, pancreatic islet function, insulin and C-peptide, blood lipid profile, body weight and BMI, etc.

    📉 Clinical Data 1: HbA1c Reduction

    Blood Glucose Management
    HbA1c reduced to below 7.0%, with a reduction of 0.73% and an attainment rate exceeding 80%.
    Trial Notes: In the test group, the HbA1c attainment rate (<7.0%) reached 80.95%, with a significant absolute reduction of 0.73% (from a baseline of 7.14%). This reduction was 2.2 times greater than that observed in the control group, and the difference was statistically significant (P=0.0260).
    This indicates that SugaRite ™ can effectively control HbA1c levels and may help prevent complications.

    Clinical Data 2: Insulin Sensitivity

    Blood Glucose Management1
    Improved insulin resistance and restored insulin sensitivity.
    Trial Notes: While achieving blood glucose control, the required levels of insulin and C-peptide in the test group were significantly lower than those in the control group. This difference became particularly pronounced after 60 days of trial consumption.
    Coupled with the significant reduction in HOMA-IR (Homeostatic Model Assessment for Insulin Resistance), these findings collectively indicate that SugaRite ™ effectively enhances the body's insulin sensitivity and can help ameliorate insulin resistance.

    ⚖️ Clinical Data 3: Weight Management

    Blood Glucose Management2
    Significant reductions in body weight and BMI, contributing to weight management.
    Trial Notes: The test group showed a significant reduction in body weight by 3.66 kg from baseline (from 72.55 kg to 68.77 kg), and a reduction in BMI by 1.41 (from 26.47 to 25.06). This improvement was nearly twice that observed in the control group, with the difference reaching statistical significance.
    It demonstrates that SugaRite ™ can promote weight loss and improvement in BMI. Body Mass Index (BMI) and Body Weight: Weight reduction itself is one of the most effective methods for improving insulin resistance.
    Clinical Report Summary
    SugaRite ™ Premix Probiotics powder can regulate blood glucose, lower HbA1c, ameliorate insulin resistance, restore insulin sensitivity, and support weight management.

    Frequently Asked Questions (FAQ)

    What are the main functions of SugaRite™ Premix Probiotics Powder?
    The main functions of SugaRite™ are to lower blood glucose, reduce body weight, and serve as an adjuvant therapy for individuals managing blood sugar levels.
    Which probiotic strains are included in SugaRite™?
    SugaRite™ contains a custom blend of functional strains: Bifidobacterium animalis subsp. lactis F1-7, Bifidobacterium animalis subsp. lactis BA-C9, Lactiplantibacillus plantarum YZX21, Lactiplantibacillus plantarum F3-2, Lactiplantibacillus plantarum H-87, and Lacticaseibacillus paracasei G15.
    What clinical evidence supports SugaRite™?
    A randomized, double-blind, placebo-controlled feeding trial was conducted with 60 Type 2 Diabetes patients over 90 days at The Second Affiliated Hospital of Zhejiang University School of Medicine. Results showed significant improvements in HbA1c, insulin resistance (HOMA-IR), and body weight.
    How effective is SugaRite™ in reducing HbA1c levels?
    Clinical data showed that the test group achieved an HbA1c attainment rate (<7.0%) of 80.95% within 90 days, with a significant absolute reduction of 0.73%. This reduction was 2.2 times greater than that observed in the control group.
    Does SugaRite™ help with weight loss?
    Yes. The clinical test group showed an average body weight reduction of 3.66 kg and an average BMI decrease of 1.41 over the 90-day trial period, which was nearly twice the improvement observed in the control group.
    What was the daily dosage protocol used in the clinical study?
    The intervention protocol used during the 90-day clinical study was 2g of the probiotics powder, consumed twice daily.

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