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THE EFFECT OF LUMBRICUS RUBELLUS DLBS1033 EXTRACT IN PATIENTS WITH TYPE 2 DIABETES MELLITUS

2026년 6월 28일 업데이트: Nabila Aushaf Prasetyo, Universitas Sebelas Maret

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

This randomized, open-label, controlled trial aims to evaluate the effect of oral Lumbricus Rubellus extract DLBS1033 as adjunctive therapy on inflammatory biomarker (hs-CRP), angiogenic factor (VEGF), and quality of life in patients with Type 2 Diabetes Mellitus. Sixty eligible patients attending the Endocrinology Outpatient Clinic of RSUD Dr. Moewardi Surakarta will be randomized into three groups: two intervention groups receiving standard DM therapy combined with DLBS1033 (490 mg t.i.d. as either 3×1 tablet or 3×2 tablets daily) and one control group receiving standard DM therapy alone, over a 4-week observation period from May to June 2026. Primary outcomes include changes in serum hs-CRP and VEGF levels; secondary outcome is health-related quality of life assessed by EQ-5D-5L.

연구 개요

상태

완전한

정황

개입 / 치료

상세 설명

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.

연구 유형

중재적

등록 (실제)

60

단계

  • 4단계

연락처 및 위치

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연구 장소

    • Central Java
      • Surakarta, Central Java, 인도네시아, 57126
        • Dr. Moewardi Regional General Hospital

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 성인
  • 고령자

건강한 자원 봉사자를 받아들입니다

아니

설명

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.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 무작위
  • 중재 모델: 병렬 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: 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
실험적: 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
위약 비교기: Control Group
Patients with Type 2 Diabetes Mellitus who received standard DM therapy alone during the 4-week observation period.
Standard Diabetes Mellitus Therapy

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
hs-CRP (High-sensitivity C-Reactive Protein)
기간: 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.
Baseline and week 4
VEGF (Vascular Endothelial Growth Factor)
기간: 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

2차 결과 측정

결과 측정
측정값 설명
기간
Quality of Life - EQ-5D-5L
기간: 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

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

스폰서

수사관

  • 수석 연구원: Nabila Aushaf Prasetyo, MD, Department of Internal Medicine, Faculty of Medicine, Universitas Sebelas Maret Surakarta

간행물 및 유용한 링크

연구에 대한 정보 입력을 담당하는 사람이 자발적으로 이러한 간행물을 제공합니다. 이것은 연구와 관련된 모든 것에 관한 것일 수 있습니다.

일반 간행물

  • 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

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (실제)

2026년 3월 1일

기본 완료 (실제)

2026년 6월 21일

연구 완료 (실제)

2026년 6월 28일

연구 등록 날짜

최초 제출

2026년 6월 28일

QC 기준을 충족하는 최초 제출

2026년 6월 28일

처음 게시됨 (실제)

2026년 7월 6일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 7월 6일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 6월 28일

마지막으로 확인됨

2026년 6월 1일

추가 정보

이 연구와 관련된 용어

기타 연구 ID 번호

  • DLBS1033 on Diabetes Mellitus

개별 참가자 데이터(IPD) 계획

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