- ICH GCP
- Реестр клинических исследований США
- Клиническое испытание NCT07684625
THE EFFECT OF LUMBRICUS RUBELLUS DLBS1033 EXTRACT IN PATIENTS WITH TYPE 2 DIABETES MELLITUS
THE EFFECT OF LUMBRICUS RUBELLUS DLBS1033 EXTRACT ON LEVELS OF HIGH-SENSITIVITY C-REACTIVE PROTEIN, VASCULAR ENDOTHELIAL GROWTH FACTOR, AND QUALITY OF LIFE IN PATIENTS WITH TYPE 2 DIABETES MELLITUS
Обзор исследования
Статус
Условия
Подробное описание
Type 2 Diabetes Mellitus (T2DM) is a major global health problem characterized by chronic hyperglycemia, persistent low-grade systemic inflammation, and vascular endothelial dysfunction. These pathological processes are central to the development of micro- and macrovascular complications, which are the leading causes of morbidity, mortality, and reduced quality of life in patients with T2DM.
Chronic hyperglycemia activates multiple pathophysiological pathways, including mitochondrial oxidative stress, the Advanced Glycation End Products (AGEs)-RAGE signaling axis, and impaired insulin signaling, collectively creating sustained systemic microinflammation and progressive endothelial damage. This endothelial dysfunction underlies the development of atherosclerosis, microcirculatory impairment, and pathological angiogenesis in T2DM patients.
High-sensitivity C-Reactive Protein (hs-CRP), a sensitive marker of systemic inflammation, is significantly elevated in T2DM and correlates with increased cardiovascular complication risk. Concurrently, Vascular Endothelial Growth Factor (VEGF), the primary mediator of endothelial cell proliferation and survival, exhibits the so-called 'VEGF paradox' in T2DM, whereby systemically elevated VEGF fails to produce functional neovascularization and instead promotes dysangiogenesis and pathological vascular permeability. These two pathways-hs-CRP-mediated inflammation and VEGF-mediated angiogenesis-interact in a mutually reinforcing pathological cycle that accelerates vascular complication progression.
Current T2DM management primarily targets glycemic control, which, while effective in reducing long-term complications, is insufficient to fully suppress chronic inflammation and correct vascular dysfunction. Adjuvant therapeutic strategies targeting non-glycemic pathogenic pathways, particularly inflammation and endothelial dysfunction, are therefore needed.
Lumbricus Rubellus extract (DLBS1033), produced by PT Dexa Medica through the Dexa Laboratories of Biomolecular Sciences (DLBS) in compliance with Good Manufacturing Practice (GMP) standards, contains low molecular weight proteins (Lumbricus Low Molecular Weight Proteins/LLP), including lumbrokinase-a serine protease enzyme with fibrinolytic, antithrombotic, and anti-inflammatory activities. Previous studies have demonstrated that lumbrokinase can suppress inflammatory mediators such as TNF-α and NF-κB, inhibit platelet aggregation, degrade fibrinogen, and improve microcirculatory function. However, its simultaneous effects on both hs-CRP and VEGF in T2DM patients remain insufficiently studied.
Eligible patients with T2DM attending the Endocrinology Outpatient Clinic of RSUD Dr. Moewardi Surakarta will be recruited consecutively and randomized using a block randomization method (fixed block size of 4) into three parallel groups: Intervention Group A (standard DM therapy + DLBS1033 490 mg t.i.d. as 3×1 tablet daily for 4 weeks), Intervention Group B (standard DM therapy + DLBS1033 490 mg t.i.d. as 3×2 tablets daily for 4 weeks), and Control Group (standard DM therapy alone). Randomization sequences will be generated independently using web-based software (www.random.org) and secured to maintain allocation concealment.
At baseline, all subjects will undergo clinical and demographic data collection, physical examination, and venous blood sampling for complete blood count, HbA1C, creatinine, SGOT, SGPT, hs-CRP (by immunoturbidimetric method), and VEGF (by Enzyme-Linked Immunosorbent Assay/ELISA). During the 4-week intervention period, biweekly follow-up visits will assess therapy adherence using the Medication Adherence Report Scale (MARS) and monitor for adverse effects. At week 4, repeat measurements of hs-CRP, VEGF, creatinine, SGOT, SGPT, MARS score, and health-related quality of life using the EQ-5D-5L questionnaire will be performed. Statistical analysis will use One-Way ANOVA (normally distributed data) or Kruskal-Wallis test (non-normally distributed data), with Analysis of Covariance (ANCOVA) and constrained Longitudinal Data Analysis (cLDA) for sensitivity analyses controlling for confounders including age, sex, nutritional status, comorbidities, and baseline biomarker values.
Тип исследования
Регистрация (Действительный)
Фаза
- Фаза 4
Контакты и местонахождение
Места учебы
-
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Central Java
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Surakarta, Central Java, Индонезия, 57126
- Dr. Moewardi Regional General Hospital
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-
Критерии участия
Критерии приемлемости
Возраст, подходящий для обучения
- Взрослый
- Пожилой взрослый
Принимает здоровых добровольцев
Описание
Inclusion Criteria:
- Patients diagnosed with Type 2 Diabetes Mellitus currently on therapy.
- Patients receiving Lumbricus Rubellus extract therapy during outpatient care at the Endocrinology Clinic.
- Adults aged >18 years, both male and female.
- Willing to undergo monthly evaluations during the 1-month study period
Exclusion Criteria:
- Patients with diabetic foot ulcer grade 1-2.
- Patients with Diabetic Kidney Disease (DKD) Stage 5.
- Patients with chronic liver disease.
- Post-operative patients.
- Patients with malignancy.
- Patients with autoimmune disease or active infection.
- Non-compliant or uncooperative patients during the monitoring period.
Учебный план
Как устроено исследование?
Детали дизайна
- Основная цель: Уход
- Распределение: Рандомизированный
- Интервенционная модель: Параллельное назначение
- Маскировка: Нет (открытая этикетка)
Оружие и интервенции
Группа участников / Армия |
Вмешательство/лечение |
|---|---|
|
Экспериментальный: Group A (Low Dose)
Patients with Type 2 Diabetes Mellitus who received oral Lumbricus Rubellus extract DLBS1033 (490 mg, DISOLF film-coated tablet, Dexa Medica, 3×1 tablet daily) combined with standard DM therapy during the 4-week observation period.
|
DLBS1033: 490 mg, DISOLF film-coated tablet, Dexa Medica, 3×1 tablet t.i.d. for 4 weeks
Standard Diabetes Mellitus Therapy
|
|
Экспериментальный: Group B (High Dose)
Patients with Type 2 Diabetes Mellitus who received oral Lumbricus Rubellus extract DLBS1033 (490 mg, DISOLF film-coated tablet, Dexa Medica, 3×2 tablets daily) combined with standard DM therapy during the 4-week observation period.
|
Standard Diabetes Mellitus Therapy
DLBS1033: 490 mg, DISOLF film-coated tablet, Dexa Medica, 3×2 tablets t.i.d. for 4 weeks
|
|
Плацебо Компаратор: Control Group
Patients with Type 2 Diabetes Mellitus who received standard DM therapy alone during the 4-week observation period.
|
Standard Diabetes Mellitus Therapy
|
Что измеряет исследование?
Первичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
|
hs-CRP (High-sensitivity C-Reactive Protein)
Временное ограничение: Baseline and week 4
|
Serum hs-CRP levels measured using immunoturbidimetric method at baseline and at week 4 post-initiation of therapy, to assess the effect of DLBS1033 on systemic inflammatory status in Type 2 Diabetes Mellitus patients.
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Baseline and week 4
|
|
VEGF (Vascular Endothelial Growth Factor)
Временное ограничение: Baseline and week 4
|
Serum VEGF levels measured using Enzyme-Linked Immunosorbent Assay (ELISA) at baseline and at week 4 post-initiation of therapy, to assess the effect of DLBS1033 on angiogenic factor regulation in Type 2 Diabetes Mellitus patients.
|
Baseline and week 4
|
Вторичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
|
Quality of Life - EQ-5D-5L
Временное ограничение: Baseline and week 4
|
Assessment of health-related quality of life using the EQ-5D-5L (EuroQol 5 Dimensions 5 Levels) instrument, comprising a five-dimension descriptive system (mobility, self-care, usual activities, pain/discomfort, anxiety/depression, each rated 1-5) and the EQ Visual Analogue Scale (EQ-VAS, 0-100).
Assessment performed at baseline and at week 4. Higher EQ-VAS scores and lower dimension levels indicate better health-related quality of life.
|
Baseline and week 4
|
Соавторы и исследователи
Спонсор
Следователи
- Главный следователь: Nabila Aushaf Prasetyo, MD, Department of Internal Medicine, Faculty of Medicine, Universitas Sebelas Maret Surakarta
Публикации и полезные ссылки
Общие публикации
- Dewi NWS, Mahendra AN. The in-vivo anti-inflammatory effect of red earthworm (Lumbricus Rubellus) ethanolic extract from organic farmland in Bali, Indonesia. Bali Med J 2020;9(3):652-655
- Öz S, Özden H, Yıldız F, et al. Protective effect of Lumbricus Rubellus Hoffmeister extract in experimental renal ischemia/reperfusion injury in the nephrectomy rats. INDIAN J Exp Biol 2023;61(December)
- Semih Oz, Yildiz F, Senturk H, et al. Protective Effects of Lumbricus Extract on the Antioxidant System and Liver in an Experimentally Created Liver Ischemia Reperfusion Injury Model in Rats. Biol Bull 2023;50(3):276-283
Даты записи исследования
Изучение основных дат
Начало исследования (Действительный)
Первичное завершение (Действительный)
Завершение исследования (Действительный)
Даты регистрации исследования
Первый отправленный
Впервые представлено, что соответствует критериям контроля качества
Первый опубликованный (Действительный)
Обновления учебных записей
Последнее опубликованное обновление (Действительный)
Последнее отправленное обновление, отвечающее критериям контроля качества
Последняя проверка
Дополнительная информация
Термины, связанные с этим исследованием
Ключевые слова
Дополнительные соответствующие термины MeSH
Другие идентификационные номера исследования
- DLBS1033 on Diabetes Mellitus
Планирование данных отдельных участников (IPD)
Планируете делиться данными об отдельных участниках (IPD)?
Сроки обмена IPD
Критерии совместного доступа к IPD
Совместное использование IPD Поддерживающий тип информации
- STUDY_PROTOCOL
- САП
- КСО
Информация о лекарствах и устройствах, исследовательские документы
Изучает лекарственный продукт, регулируемый FDA США.
Изучает продукт устройства, регулируемый Управлением по санитарному надзору за качеством пищевых продуктов и медикаментов США.
Эта информация была получена непосредственно с веб-сайта clinicaltrials.gov без каких-либо изменений. Если у вас есть запросы на изменение, удаление или обновление сведений об исследовании, обращайтесь по адресу register@clinicaltrials.gov. Как только изменение будет реализовано на clinicaltrials.gov, оно будет автоматически обновлено и на нашем веб-сайте. .