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Effect of HMP on Diabetic Microangiopaemia in T2DM

Effect of Heart-Protecting Musk Pill on Diabetic Microangiopaemia in Type 2 Diabetes Patients

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05095922
Enrollment
40
Registered
2021-10-27
Start date
2023-03-28
Completion date
2024-05-30
Last updated
2024-07-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetes Mellitus, Type 2, Diabetic Angiopathies

Keywords

Heart-protecting musk pill, type 2 diabetes, diabetic angiopathies

Brief summary

The study mainly investigates the therapeutic effect of Heart-Protecting Musk Pill (HMP) on patients with diabetic microangiopathy. According to the indicators of diabetic nephropathy (DN), diabetic retinopathy (DR), oxidative stress and inflammatory factor in patients with diabetic microvascular disease after using HMP, the investigators aim to evaluate the effect of HMP on diabetic microangiopathy, oxidative stress and inflammation.

Detailed description

Diabetes can lead to many diseases as diabetic macrovascular and microvascular complications which result in high disability and mortality rate, thereby seriously affecting the quality of life and life expectancy of diabetic patients. It not only aggravates the family burden of patients, but also becomes the main burden of public health services around the world. Diabetic nephropathy (DN) and diabetic retinopathy (DR) are more serious in diabetic microangiopathy. The glomerulus and retina have the similar tissue structure and physiological function. Therefore, when they are exposured to the same risk factors can lead to microcirculation damage of kidney and retina. DN and DR have similar pathogenesis and development processes. Although the susceptibility genes and cytokines of DN and DR are different, the two can still be predictors of each other and they often coexist in diabetic patients. At present, there are few drugs with definite curative effect on the treatment of diabetic microangiopathy, therefore the treatment of diabetic microangiopathy is an aspect that urgently needs a breakthrough in chronic complications of diabetes. Traditional Chinese medicine has a history of preventing and treating diabetes for thousands of years. For the treatment of chronic complications of diabetes by Chinese medicine, although there are not many Chinese medicines that have obtained curative effects, it has indeed accumulated rich experience in the process of research and clinical treatment that Western medicine could not obtain. Therefore, seeking Chinese medicine to effectively treat diabetic microvascular disease has become a direction worthy of attention and research. Heart-Protecting Musk Pill (HMP) is a commonly used drug in clinical treatment, which comprises seven medicinal substances: Radix Ginseng, Venenum Bufonis, Styrax, Calculus Bovis Artifactus, Cortex Cinnamomi, Borneolum Syntheticum and Artificial Moschus. HMP is a traditional Chinese medicinal compound, which has been effectively used for treating coronary heart disease (CHD) and diabetic macrovascular disease. However, studies on Chinese medicines that are partially similar to HMP have shown that they can improve diabetic retinopathy. Therefore, the study of the efficacy of HMP on diabetic microangiopathy is extremely valuable. Previous researches have shown that HMP owns the effects of reducing oxidative stress, improving inflammation, anti-plateleting aggregation, promoting plasmin activity, and improving hemodynamics. It is possible that HMP can delay or improve the occurrence and development of diabetic microangiopathy through the above effects and even other unclear mechanisms. At present, the drugs used for clinical treatment of type 2 diabetic microangiopathy are limited. Although the pharmacological indications of HMP can be used to deal with the pathogenesis of diabetic microvascular complications, there is still no clinical study of HMP for the treatment of diabetic microvascular complications. Therefore, this study compared the differences in indicators related to diabetic nephropathy, diabetic retinopathy, oxidative stress, and inflammatory factors between the control group and the HMP group before and after treatment to clarify the therapeutic effect of HMP on diabetic microangiopaemia.

Interventions

Heart-Protecting Musk Pill (pill, 45mg, three times a day, 3 months)

Valsartan Capsules(capsule, 80mg, once a day, 3 months)

Calcium Dobesilate Capsules(capsule, 500mg, three times a day, 3 months)

Sponsors

Affiliated Hospital of Nantong University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

The type 2 diabetes subjects with diabetic microangiopathy

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* Clinical diagnosis of Diabetes mellitus * Prescribed for Valsartan Capsules and Calcium Dobesilate Capsules

Exclusion criteria

* Type 1 diabetes mellitus * Secondary diabetes * Malignant tumors * Active infection * Acute diabetic complications * Macrovascular complications * Mental illness * Intellectual disability * Impaired heart function * Impaired liver function * Impaired kidney function

Design outcomes

Primary

MeasureTime frameDescription
Concentration of biochemical IndicatorsChange from Baseline TC, TG, HDL-C, LDL-C, FBG, BUN at 3 monthsTotal cholesterol(TC), Triglycerides(TG), High-density lipoprotein cholesterol(HDL-C), Low-density lipoprotein cholesterol(LDL-C), Fasting blood glucose(FBG), Blood urea nitrogen(BUN)
Concentration of Glycosylated hemoglobinChange from Baseline HbA1c at 3 monthsGlycosylated hemoglobin(HbA1c)
Concentration of hypersensitive-c-reactive-protein and Cystatin CChange from Baseline hs-CRP and CysC at 3 monthshypersensitive-c-reactive-protein(hs-CRP), Cystatin C(CysC)
Concentration of Serum creatinineChange from Baseline Scr at 3 monthsSerum creatinine(Scr)
Rate of estimated Glomerular FiltrationChange from Baseline eGFR at 3 monthsestimated Glomerular Filtration Rate(eGFR)
Ratio of Urinary albumin to creatinineChange from Baseline UACR at 3 monthsUrinary albumin to creatinine Ratio(UACR)
Concentration of Serum fatty acid binding protein 4Change from Baseline FABP4 at 3 monthsSerum fatty acid binding protein 4(FABP4)
Indicators of diabetic retinopathyChange from Baseline effect at 3 monthsThe vision and fundus photography will be checked by an ophthalmologist to determine the effect.
Concentration of inflammation indicatorChange from Baseline TNF-α at 3 monthsTumor Necrosis Factor-α(TNF-α)
Concentration of Oxidative stress indicatorChange from Baseline SOD at 3 monthsSuperoxide dismutase(SOD)
Clinical characteristicsChange from Baseline Height, Waistline at 3 monthsHeight, Waistline
Clinical characteristicChange from Baseline Weight at 3 monthsWeight
Blood pressureChange from Baseline SBP, DBP at 3 monthsSystolic Blood Pressure(SBP), Diastolic Blood Pressure(DBP)

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026