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Beraprost Sodium and Arterial Stiffness in Patients With Type 2 Diabetic Nephropathy

Primary Purpose

Diabetic Nephropathy

Status
Unknown status
Phase
Not Applicable
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Beraprost sodium
Sponsored by
Seoul National University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetic Nephropathy

Eligibility Criteria

20 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Aged 19 years or more and 75 years or less
  • Type 2 diabetes who is prescribed glucose-lowering agent or insulin
  • Estimated glomerular filtration rate (GFR) by isotope dilution mass spectrometry (IDMS)- Modification of Diet in Renal Disease (MDRD) equation 30 ml/min/1.73 m2 or more
  • verified 2 times or more of albuminuria 30 mg/g cr (or protein 300 mg/g cr)or more in a spot urine sample with interval of 1 week or more in recent 6 months
  • Patients whose blood pressure is 140/90 mmHg or less and did not receive a prescription for additional antihypertensive medication in recent 3 months
  • Patients who give written consent to this study by oneself

Exclusion Criteria:

  • History of kidney transplantation
  • current advanced congestive heart failure (NYHA class III or more)
  • current uncontrolled arrhythmia
  • current advanced liver cirrhosis (Child-Pugh class C)
  • History of bleeding diathesis
  • current active infection or uncontrolled inflammatory disorders
  • History of cerebrovascular accident or myocardial infarction
  • current use of anticoagulant
  • current use of two or more antiplatelet agents
  • patients with advanced malignancy (life expectancy less than 6 months)
  • patients with uncontrolled diabetes (Hba1c more than 10%)
  • patients with severe anemia (Hb less than 8.0 g/dL)
  • female who are pregnant, trying to get pregnant or lactating
  • Genetic diseases such as galactose intolerance, lactose deficiency or glucose-galactose malabsorption

Sites / Locations

  • Hallym University Sacred Heart HospitalRecruiting
  • Seoul National University Bundang HospitalRecruiting
  • Kangnam Sacred Heart HospitalRecruiting
  • Seoul National University Boramae Medical CenterRecruiting
  • Seoul National University HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Beraprost sodium

Placebo

Arm Description

Beraprost sodium 0.02 mg capsule by mouth every 12 hours for 12 weeks

Placebo capsule by mouth every 12 hours for 12 weeks

Outcomes

Primary Outcome Measures

Brachial ankle pulse wave velocity (PWV)
The change of brachial ankle PWV at 12 weeks compared to baseline (0 week)

Secondary Outcome Measures

Ankle brachial indices (ABI)
The change of ABI at 12 weeks compared to baseline (0 week)
Urine albumin creatinine ratio (UACR)
The change of UACR at 12 weeks compared to baseline (0 week)
IDMS MDRD estimated glomerular filtration rate (eGFR)
The change of IDMS MDRD eGFR at 12 weeks compared to baseline (0 week)
Lipid profiles
The change of total cholesterol, LDL-cholesterol, and triglyceride at 12 weeks compared to baseline (0 week)
Blood pressure
The change of systolic and diastolic blood pressure at 12 weeks compared to baseline (0 week)

Full Information

First Posted
February 19, 2013
Last Updated
December 13, 2013
Sponsor
Seoul National University Hospital
Collaborators
Astellas Pharma Korea, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT01796418
Brief Title
Beraprost Sodium and Arterial Stiffness in Patients With Type 2 Diabetic Nephropathy
Official Title
Effect of Beraprost Sodium on Arterial Stiffness in Patients With Type 2 Diabetic Nephropathy (BESTinDN Study)
Study Type
Interventional

2. Study Status

Record Verification Date
December 2013
Overall Recruitment Status
Unknown status
Study Start Date
March 2013 (undefined)
Primary Completion Date
August 2014 (Anticipated)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Seoul National University Hospital
Collaborators
Astellas Pharma Korea, Inc.

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Diabetic nephropathy, the leading cause of end-stage renal disease in many countries, is characterized by high cardiovascular mortality and morbidity even in the early course of the disease. In addition, cardiovascular complication has been the most common cause of death in these patients. Thus, early detection and appropriate intervention for this highly common and critical complication is considered to play an important role in the management of the disease. In this regard, much interest has been focused on the early markers which can predict arterial diseases before the clinically apparent cardiovascular diseases. Recently, glowing evidence suggests that arterial stiffness as assessed by pulse wave velocity (PWV) may serve as a surrogate marker for future cardiovascular disease. In fact, increased PWV has been known to be independently associated with diabetic nephropathy in type 2 diabetes. Beraprost sodium (BPS) is a stable orally active prostacyclin (PGI2) analogue that has a potent vasodilatory and anti-platelet effect. Also, BPS has been suggested to improve a micro-vascular circulation through a reduction of red blood cell deformability. In addition, recent studies have demonstrated that BPS improves endothelial function through an increase in endothelial nitric oxide synthesis and NO synthase gene transcription. These beneficial effects of BPS have been known to reduce PWV in patients prone to cardiovascular diseases such as elderly, hypertension, or a history of cerebral infarction. However, the effect of BPS on arterial stiffness in patients with diabetic nephropathy remains elusive. Our study will address the effect of BPS on arterial stiffness by PWV in patients with diabetic nephropathy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetic Nephropathy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
102 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Beraprost sodium
Arm Type
Experimental
Arm Description
Beraprost sodium 0.02 mg capsule by mouth every 12 hours for 12 weeks
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo capsule by mouth every 12 hours for 12 weeks
Intervention Type
Drug
Intervention Name(s)
Beraprost sodium
Other Intervention Name(s)
Berasil
Primary Outcome Measure Information:
Title
Brachial ankle pulse wave velocity (PWV)
Description
The change of brachial ankle PWV at 12 weeks compared to baseline (0 week)
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Ankle brachial indices (ABI)
Description
The change of ABI at 12 weeks compared to baseline (0 week)
Time Frame
12 weeks
Title
Urine albumin creatinine ratio (UACR)
Description
The change of UACR at 12 weeks compared to baseline (0 week)
Time Frame
12 weeks
Title
IDMS MDRD estimated glomerular filtration rate (eGFR)
Description
The change of IDMS MDRD eGFR at 12 weeks compared to baseline (0 week)
Time Frame
12 weeks
Title
Lipid profiles
Description
The change of total cholesterol, LDL-cholesterol, and triglyceride at 12 weeks compared to baseline (0 week)
Time Frame
12 weeks
Title
Blood pressure
Description
The change of systolic and diastolic blood pressure at 12 weeks compared to baseline (0 week)
Time Frame
12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Aged 19 years or more and 75 years or less Type 2 diabetes who is prescribed glucose-lowering agent or insulin Estimated glomerular filtration rate (GFR) by isotope dilution mass spectrometry (IDMS)- Modification of Diet in Renal Disease (MDRD) equation 30 ml/min/1.73 m2 or more verified 2 times or more of albuminuria 30 mg/g cr (or protein 300 mg/g cr)or more in a spot urine sample with interval of 1 week or more in recent 6 months Patients whose blood pressure is 140/90 mmHg or less and did not receive a prescription for additional antihypertensive medication in recent 3 months Patients who give written consent to this study by oneself Exclusion Criteria: History of kidney transplantation current advanced congestive heart failure (NYHA class III or more) current uncontrolled arrhythmia current advanced liver cirrhosis (Child-Pugh class C) History of bleeding diathesis current active infection or uncontrolled inflammatory disorders History of cerebrovascular accident or myocardial infarction current use of anticoagulant current use of two or more antiplatelet agents patients with advanced malignancy (life expectancy less than 6 months) patients with uncontrolled diabetes (Hba1c more than 10%) patients with severe anemia (Hb less than 8.0 g/dL) female who are pregnant, trying to get pregnant or lactating Genetic diseases such as galactose intolerance, lactose deficiency or glucose-galactose malabsorption
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Chun-Soo Lim, Prof
Phone
82-2-870-2120
Email
cslimjy@snu.ac.kr
First Name & Middle Initial & Last Name or Official Title & Degree
Dong Ki Kim, Prof
Phone
82-2-2072-2303
Email
dkkim73@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Chun-Soo Lim, Prof
Organizational Affiliation
Department of Internal Medicine, Seoul National University Boramae Medical Center, Seoul, Korea
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Dong Ki Kim, Prof
Organizational Affiliation
Department of Internal Medicine, Seoul National University Hospital, Seoul, Korea
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ki Young Na, Prof
Organizational Affiliation
Department of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Sung Gyun Kim, Prof
Organizational Affiliation
Hallym University Medical Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Young-Ki Lee, Prof
Organizational Affiliation
Hallym University Kangnam Sacred Heart Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hallym University Sacred Heart Hospital
City
Anyang
Country
Korea, Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sung Gyun Kim, Prof
Phone
82-31-380-3728
Email
sgkim@hallym.ac.kr
First Name & Middle Initial & Last Name & Degree
Sung Gyun Kim, Prof
Facility Name
Seoul National University Bundang Hospital
City
Seongnam
Country
Korea, Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ki Young Na, Prof
Email
kyna@snubh.org
First Name & Middle Initial & Last Name & Degree
Ki Young Na, Prof
Facility Name
Kangnam Sacred Heart Hospital
City
Seoul
Country
Korea, Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Young-Ki Lee, Prof
Phone
82-2-829-5114
Email
km2071@naver.com
First Name & Middle Initial & Last Name & Degree
Young-Ki Lee, Prof
Facility Name
Seoul National University Boramae Medical Center
City
Seoul
Country
Korea, Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Chun-Soo Lim, Prof
Phone
82-2-872-2120
Email
cslimjy@snu.ac.kr
First Name & Middle Initial & Last Name & Degree
Chun-Soo Lim, Prof
Facility Name
Seoul National University Hospital
City
Seoul
Country
Korea, Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dong Ki Kim, Prof
Phone
82-2-2072-2303
Email
dkkim73@gmail.com
First Name & Middle Initial & Last Name & Degree
Dong Ki Kim, Prof

12. IPD Sharing Statement

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Beraprost Sodium and Arterial Stiffness in Patients With Type 2 Diabetic Nephropathy

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