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DLBS1033 Treatment in Diabetic With Peripheral Arterial Disease

Phase 2
Terminated
Conditions
Diabetes
Peripheral Arterial Disease
Interventions
Drug: Placebo
Registration Number
NCT02145988
Lead Sponsor
Dexa Medica Group
Brief Summary

This is a prospective, randomized, double-blind, double-dummy, and controlled study of DLBS1033 for the improvement of ankle-brachial index in diabetic patients with peripheral arterial disease (PAD). It is hypothesized that the addition of DLBS1033 on top of aspirin treatment will augment significantly the resting ABI in diabetes patient with PAD in comparison with that of aspirin alone.

Detailed Description

Subjects in this study will be screened consecutively and eligible subjects will be randomized to receive aspirin tablet 80 mg once daily and either the investigational drug (DLBS1033 tablet 490 mg three times daily) or its placebo, for 12 weeks.

Diabetic subjects who have been being under therapy with aspirin can directly start with study treatment. For those who are currently not under therapy with aspirin, there will be a run-in period during which they will receive (or be switched to) aspirin treatment, for two weeks. After then, they will receive study medication.

Clinical and laboratory examinations to evaluate the investigational drug's efficacy and safety will be performed at baseline and at the interval of six weeks over the twelve week-course of therapy.

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
11
Inclusion Criteria
  • Signed informed consent before any trial related activities.
  • Male or female subjects of 40 - 65 years of age.
  • Diagnosis of diabetes mellitus defined as HbA1c level of ≥ 6.5% (for newly diagnosed diabetes) or based on medical history.
  • Presence of peripheral arterial disease with resting ankle-brachial index (ABI) of 0.41-0.90 inclusive
Exclusion Criteria
  • Females of childbearing potential: pregnancy, breast-feeding, and the intention of becoming pregnant.
  • Recent stroke attack, myocardial infarction/unstable angina/acute coronary syndrome, coronary artery bypass surgery (CABG) or percutaneous transluminal coronary angioplasty (PTCA)/stent within 3 (three) months prior to screening.
  • Impaired liver function: serum ALT > 2.5 times upper limit of normal.
  • Impaired renal function: serum creatinine ≥ 1.5 times upper limit of normal.
  • Concomitant use of other antithrombosis drugs or any antiplatelets other than the study medication.
  • Subjects with concurrent herbal (alternative) medicines or food supplements
  • Subjects with any other disease state, including chronic or acute systemic infections, uncontrolled illnesses or other chronic diseases, which judged by the investigator, could interfere with trial participation or trial evaluation.
  • Subjects with high risk of bleeding:
  • Subjects with prior experience with DLBS1033 or other oral lumbrokinase products.
  • Subjects with known or suspected allergy to any of study medications used in the study, including other lumbrokinase products.
  • Subjects with known or suspected allergy or resistant to aspirin.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
DLBS1033DLBS1033DLBS1033 tablet is administered at the dose of 490 mg, one tablet three times daily, every day for twelve weeks of study period
PlaceboPlaceboPlacebo tablet is administered one tablet three times daily, every day for twelve weeks of study period
Primary Outcome Measures
NameTimeMethod
Resting ankle-brachial index (ABI)Week 0 and 12

The change of resting ABI

Secondary Outcome Measures
NameTimeMethod
Adverse eventsWeek 0 - 12

Adverse events, including bleeding events, will be observed and carefully evaluated along the course of the study

Resting ABIWeek 0 and 6

The change of resting ABI

Thromboxane B2Week 0, 6, and 12

The change of thromboxane B2

d-dimerWeek 0, 6, and 12

The change of d-dimer

Liver functionWeek 0 and 12

Liver function measured includes: serum ALT, AST, and alkaline phosphatase

Renal functionWeek 0 and 12

Renal function measured includes: serum creatinine and blood urea nitrogen (BUN)

hs-CRPWeek 0, 6, and 12

The change of hs-CRP

FibrinogenWeek 0, 6, and 12

The change of fibrinogen

Routine hematologyWeek 0, 6, and 12

Routine hematology measured includes: hemoglobin, hematocrit, RBC, WBC, differentiation of WBC, and platelet count

Haemostasis parametersWeek 0, 6, and 12

Haemostasis parameters measured includes: prothrombin time (PT) and activated partial thromboplastin time (aPTT)

Trial Locations

Locations (2)

Department of Internal Medicine, Faculty of Medicine, University of Udayana/Sanglah Hospital

🇮🇩

Denpasar, Bali, Indonesia

Department of Internal Medicine, RSUD Wangaya

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Denpasar, Bali, Indonesia

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