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临床试验/NCT06224803
NCT06224803已完成不适用

Evaluation of Effects of Dibifree® on Regulation of Blood Sugar and HbA1c in Patients With Type II Diabetes

Global Preventive Medicine Biotech Co., Ltd.2 个研究点 分布在 1 个国家目标入组 56 人开始时间: 2020年8月26日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
56
试验地点
2
主要终点
Concentration of HbA1c

研究概览

简要总结

At present, diabetic patients mainly use drugs to control blood sugar. However, drugs have side effects and the control effect varies among individuals. Even if diabetic patients can control their blood sugar well, long-term medication will still cause a series of complications, including retinopathy, nephropathy, diabetic foot, heart disease, etc. Vascular disease issues, etc.

This study will focus on the changes in HbA1c and blood sugar in patients with confirmed diabetes after taking "Dibifree®" food supplement.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
20 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age: 20 years old (inclusive) or above, gender is not restricted
  • Diagnosed with type 2 diabetes
  • HbA1c > 6.5%
  • Coagulation function and platelets are normal
  • Participants voluntarily join this treatment course and sign the informed consent form
  • Not taking other supplements containing blood sugar regulating properties for at least one month

排除标准

  • Women who are pregnant, lactating or planning to have children
  • Have factors that significantly affect the absorption of oral drugs, such as inability to swallow, chronic diarrhea, intestinal obstruction, etc.
  • Uncontrolled hypertension (>180/110 mmHG)
  • People suffering from stroke, elderly dementia, Alzheimer's disease and other brain diseases
  • During this study, the subject used other drugs or treatments that may interfere with this study in addition to blood sugar control medications.
  • GOT>4 times normal value; GPT>4 times normal value
  • Creatinine>4 times the highest normal value
  • Those who are determined by the project administrator to be unfit to participate in this clinical study

结局指标

主要结局

Concentration of HbA1c

时间窗: HbA1c was measured at baseline (V0) and during follow-up visits at months 3 (V3), 4 (V4), and 7 (V7) after intervention.

Hemoglobin A1c (HbA1c) levels were measured at baseline (V0) and routinely monitored at the third (V3), fourth (V4), and seventh (V7) months. For longitudinal analysis, repeated measures were evaluated using two-way ANOVA followed by Sidak's multiple comparisons test to assess time and treatment effects. Data are presented as mean ± SD. All statistical analyses were performed using GraphPad Prism 10 (GraphPad Software, San Diego, CA, USA). All data were considered statistically significant at p ≤ 0.05.

Body Weight and BMI

时间窗: Body weight and BMI were measured at baseline (V0) and at the end of the 7-month intervention (V7).

Changes in body weight and BMI between baseline (V0) and month 7 (V7) were analyzed using an unpaired t-test. Statistical analyses were conducted using GraphPad Prism 10 (GraphPad Software, San Diego, CA, USA), with p ≤ 0.05 considered statistically significant.

次要结局

  • Concentration of blood lipid(The measurement at baseline (V0) and during follow-up visits at months 3 (V3), 4 (V4), and 7 (V7) after intervention.)
  • Concentration of Blood Sugar(measured at baseline (V0) and during follow-up visits at months 3 (V3), 4 (V4), and 7 (V7) after intervention.)
  • Kidney Function Parameters: BUN, Creatinine, and eGFR(Kidney function parameters measured at baseline (V0) and during follow-up visits at months 3 (V3), 4 (V4), and 7 (V7) after intervention.)
  • Liver Function Parameters: GOT and GPT(Liver function parameters measured at baseline (V0) and during follow-up visits at months 3 (V3), 4 (V4), and 7 (V7) after intervention.)

研究者

发起方
Global Preventive Medicine Biotech Co., Ltd.
申办方类型
Industry
责任方
Sponsor

研究点 (2)

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