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Buyuan-zhixiao Formula in the Treatment of Elderly Patients With Diabetes and Multiple Metabolic Disorders

Not Applicable
Not yet recruiting
Conditions
Diabete Mellitus
Aging
Metabolic Disorders
Traditional Chinese Medicine
Randomized Controlled Trial
Interventions
Drug: Placebo
Drug: Buyuan Zhixiao Formula
Registration Number
NCT06358118
Lead Sponsor
Qing Ni
Brief Summary

The primary objective of this clinical trial is to assess the clinical efficacy and safety of the Buyuan Zhixiao Formula in treating elderly patients with diabetes and multiple metabolic disorders exhibiting symptoms of renal deficiency and blood stasis. Furthermore, this study aims to intervene in high-risk factors to prevent arteriosclerosis and to investigate the clinical efficacy of the Buyuan Zhixiao Formula in the prevention and treatment of cognitive impairments.

The main questions it aims to answer are:

1. What are the clinical effects of Buyuan Zhixiao Formula, including lowering blood sugar, lowering blood pressure, lowering lipids, and treating obesity?

2. Can Buyuan Zhixiao Formula improve cognitive impairment in diabetes? Researchers compared Buyuan Zhixiao Formula with a placebo (a drug that looks similar but contains only 10% of the active ingredients) to see if the drug Buyuan Zhixiao Formula can treat elderly people with diabetes and multiple metabolic disorders.

Participants will:

1. Take the drug Bu Yuan Zhi XiaoFormula or placebo every day for 6 months;Follow-up for 6 months;

2. Check fasting blood sugar and 2-hour postprandial blood sugar every month; check HbA1c, blood lipids, vascular function, and cognitive impairment serum markers every 3 months;

3. Conduct scores on TCM symptoms, cognitive ability, nutritional status and other scales and adverse events;

4. Urine and serum samples were collected before and after treatment;

Detailed Description

Not available

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
240
Inclusion Criteria
  • 1.Age ≥65 years, irrespective of sex;
  • 2.Individuals who meet the Western medical diagnostic criteria for type 2 diabetes mellitus (T2DM) in the elderly, with a hemoglobin A1c level of ≥7.0% in the past three months;
  • 3.Compliance with the diagnostic criteria for abdominal obesity (waist circumference ≥90 cm for males and ≥85 cm for females);
  • 4.Conformity to the diagnostic standards for hypertension (systolic blood pressure ≥140 mmHg and/or diastolic blood pressure ≥90 mmHg);
  • 5.A history of dyslipidemia, where lipid levels have not reached the general control standards for elderly individuals with T2DM following oral lipid-lowering therapy (statins/bile acid sequestrants): LDL cholesterol <2.6 mmol/L and/or triglycerides <2.5 mmol/L;
  • 6.Diagnosis of kidney deficiency and blood stasis according to traditional Chinese medicine, with the pattern type referring to the《Guidelines for Clinical Research of New Chinese Medicines》;
  • 7.Willingness to sign an informed consent document.
Exclusion Criteria
  • 1.Exclusion of individuals who, within the past week, have experienced severe infections, acute cardiovascular or cerebrovascular events (such as acute cerebral infarction or myocardial infarction), significant trauma, acute pancreatitis, or other conditions that could precipitate stress-induced hyperglycemia. This also extends to those with concurrent endocrinopathies that may induce insulin resistance, such as Cushing's syndrome, hyperthyroidism, or pituitary growth hormone adenomas, as well as those currently receiving treatment with glucocorticoids or undergoing chemotherapy for malignancies.
  • 2.Exclusion of individuals with a history of neurological disorders or psychiatric conditions that could impair cognitive function, as well as those with a history of medication use for these conditions.
  • 3.Exclusion of individuals with severe complications of diabetes such as diabetic nephropathy in the uremic stage, or those with significant primary diseases of the cardiovascular, cerebrovascular, hepatic, renal, or hematopoietic systems, as well as individuals diagnosed with cancer.
  • 4.Exclusion of individuals with communication barriers that could affect the assessment of cognitive function, including severe impairments in speech, vision, and hearing.
  • 5.Individuals who have participated in other pharmacological clinical trials within the past month.
  • 6.Individuals who have insufficient understanding of this study, are unwilling to participate, or, based on the researchers' judgment, present a reduced likelihood of enrollment or poor compliance due to unstable work and living locations or other factors that could lead to loss to follow-up.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
control groupPlaceboTake a placebos
experimental groupBuyuan Zhixiao FormulaTake Buyuan Zhixiao Formula granules
Primary Outcome Measures
NameTimeMethod
HbA1cMeasured at 0, 3, 6, and 12 months respectively.

unit:%

Secondary Outcome Measures
NameTimeMethod
TriglyceridesMeasured at 0, 3, 6, and 12 months

unit:mmol/l

BMIMeasured at 0, 1, 2, 3, 4, 5, 6, 9, and 12 months respectively

unit:kg/m2

2-hour postprandial blood glucoseMeasured at 0, 1, 2, 3, 4, 5, 6, 9, and 12 months respectively

unit:mmol/l

weightMeasured at 0, 1, 2, 3, 4, 5, 6, 9, and 12 months respectively

unit:KG

waist circumferenceMeasured at 0, 1, 2, 3, 4, 5, 6, 9, and 12 months respectively

unit:cm

Fasting blood glucoseMeasured at 0, 1, 2, 3, 4, 5, 6, 9, and 12 months respectively

unit:mmol/l

blood pressureMeasured at 0, 1, 2, 3, 4, 5, 6, 9, and 12 months respectively

unit:mmHg

Average Concentration of Interleukin-6Measured at 0, 3, 6, and 12 months
Concentration Variation of Von Willebrand FactorMeasured at 0, 3, 6, and 12 months
Average Concentration of Soluble Intercellular Adhesion Molecule-1Measured at 0, 3, 6, and 12 months
Change in Serum Tau Protein LevelsMeasured at 0, 3, 6, and 12 months
Activities of Daily Living Scale scoreMeasured at 0, 3, 6, and 12 months

The scale consists of 10 items, with a total score of 100 points. The Cronbach's alpha of the scale is 0.813. A score of 100 points is considered normal, while scores below 100 indicate a decline.A score of 100 points indicates full independence in daily living, without any dependency; 61-99 points suggest mild dependency; 41-60 points indicate moderate dependency;

≤40 points denote severe dependency.

Serum and urine metabolomicsMeasured at 0 and 6 months respectively

Inferring the potential biological mechanisms of the effect of Buyuan Zhixiao Formula based on the differences in metabolic products in the blood and urine between the experimental and control groups.

islet β-cell function indexMeasured at 0, 3, 6, and 12 months
visceral adiposity indexMeasured at 0, 3, 6, and 12 months
Measurement Results of Tumor Necrosis Factor-alpha Levels at Different Time PointsMeasured at 0, 3, 6, and 12 months
Total CholesterolMeasured at 0, 3, 6, and 12 months

unit:mmol/l

Low density lipoprotein cholesterolMeasured at 0, 3, 6, and 12 months

unit:mmol/l

lipid Lipid accumulation productMeasured at 0, 3, 6, and 12 months
Concentration Variation of Interleukin-10Measured at 0, 3, 6, and 12 months
Change in Homocysteine LevelsMeasured at 0, 3, 6, and 12 months
Average Concentration of Aβ42Measured at 0, 3, 6, and 12 months
Change in Neurofilament Light Chain Protein LevelsMeasured at 0, 3, 6, and 12 months
Montreal Cognitive Assessment ScoreMeasured at 0, 3, 6, and 12 months

The maximum score is 30 points, and the higher the score, the better the cognitive function.

Fried Frailty Phenotype ScaleMeasured at 0, 3, 6, and 12 months

Those who have 5 or more of the items in the table can be diagnosed as frailty syndrome; those with less than 3 items are in the early stage of frailty; 0 items are healthy elderly people without frailty.

Mini Nutritional Rating ScaleMeasured at 0, 3, 6, and 12 months

The total score is 14 points, with the Cronbach's alpha of the scale being 0.906. A score of ≤7 points is considered malnourished, 8-11 points indicate a risk of malnutrition, and 12-14 points are indicative of normal nutrition.

The total score is 14 points, with the Cronbach's alpha of the scale being 0.906. A score of ≤7 points is considered malnourished, 8-11 points indicate a risk of malnutrition, and 12-14 points are indicative of normal nutrition.

Ankle-Brachial Index(ABI)Measured at 0, 3, 6, and 12 months

The normal range for the ABI is generally considered to be from 0.9 to 1.3.

Fasting insulinMeasured at 0, 3, 6, and 12 months

unit:pmol/L

Change in Matrix Metalloproteinase-9 Levels" or "Participants' Matrix Metalloproteinase-9 ConcentrationMeasured at 0, 3, 6, and 12 months
Average Concentration of Aβ40Measured at 0, 3, 6, and 12 months
High density lipoprotein cholesterolMeasured at 0, 3, 6, and 12 months

unit:mmol/l

C-peptideMeasured at 0, 3, 6, and 12 months

unit:pmol/L

insulin resistance indexMeasured at 0, 3, 6, and 12 months
Change in Endothelin-1 LevelsMeasured at 0, 3, 6, and 12 months
Average Concentration of Nitric OxideMeasured at 0, 3, 6, and 12 months
Measurement Results of Vascular Endothelial Growth Factor Levels at Different Time PointsMeasured at 0, 3, 6, and 12 months
Carotid Ultrasound; Carotid Intima-Media Thickness.Measured at 0, 6, and 12 months
Activities of Daily Living Scale score; Fried Frailty Phenotype Scale; Mini Nutritional Rating Scale; MoCA scale score; Traditional Chinese Medicine Kidney Deficiency and Blood Stasis Syndrome Scale score.Measured at 0, 3, 6, and 12 months

Trial Locations

Locations (6)

Cangzhou integrative medicine hospital

🇨🇳

Hebei, China

China Academy of Chinese Medical Sciences Guang'anmen Hospital

🇨🇳

Beijin, Beijing, China

Hohhot Mongolian Traditional Chinese Medicine Hospital

🇨🇳

Neimeng, China

Binzhou Traditional Chinese Medicine Hospital

🇨🇳

Shandong, China

Yantai Baishi Traditional Chinese Medicine Hospital

🇨🇳

Shandong, China

The First Teaching Hospital of Tianjin University of Traditional Chinese Medicine

🇨🇳

Tianjin, China

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