Clinical Trial Technology Development for the Validation of Surrogate Prognostic Markers in Patients With Diabetic Nephropathy

Sponsor

Seoul National University Hospital (Other)

Overall Status

Unknown status

CT.gov ID

NCT01673204

Collaborator

(none)

276

Enrollment

Locations

Arms

138

Patients Per Site

Study Details

Study Description

Brief Summary

Worldwide, the most common cause of chronic kidney disease (CKD) and end stage renal disease (ESRD) is diabetes. Unlike the past, in south korea, diabetes account for more than 40% of ESRD. According to WHO reports in 1998, 100 million people had type 2 diabetes in 1997, and there is expected to increase by 300 million people in 2025. In addition, the expected survival time of patients with diabetes increase compared to previous. In the future, ESRD due to type 2 diabetes is expected to have a significant impact on the health industry. Therefore, prevention of progression to CKD and ESRD in diabetic patients is important to aspect of national health and economic problems. How to stop the progression of diabetic nephropathy is part of modern medicine to be solved.

Strict glycemic control, blood pressure regulation, and use of renin-angiotensin system (RAS) blockers inhibit the development and progression of diabetic nephropathy. Microalbuminuria in diabetic patients has been recognized as a predictor of progression of diabetic nephropathy. Thus, the prevention of elevated urinary albumin excretion is an important therapeutic target for the prevention of renal and cardiovascular events.

In patients with diabetes and hypertension, the drugs that block the RAS are used to treat proteinuria, but still a large number of patients with proteinuria are uncontrolled. In addition, ACE inhibitors or ARB agents actually have a limited effect on reducing the risk of cardiovascular or renal outcome. Also, sulodexide or pentoxyphylline which is reducing proteinuria have some weak evidence in terms of efficacy and safety. Therefore, the introduction of new alternative drugs are required.

Already several study reported that calcitriol or paricalcitol in the renal injury model have renopreventive effect. In addition, in diabetic renal injury mice model reported that vitamin D receptor deficiency leads to glomerulosclerosis. Inhibition of the RAS with combination of paricalcitol and RAS inhibitors effectively prevent renal injury in diabetic nephropathy. Recently, Dick de Zeeuw et al reported that addition of paricalcitol to RAS inhibition safely lower residual albuminuria in patients with diabetic nephropathy. Recent studies reported that elevated concentrations of serum markers of the TNFα and Fas-pathways are strongly associated with decreased renal function in diabetic patients. However, the role of these markers in early progressive renal function decline are not clear. Therefore, the objective of this study is to identify the renoprotective effect as an new treatment of activated vitamin D (Calcitriol) indicating the TNF-α-related anti-inflammatory action and to seek the role as an important biomarker that the changes of TNFR in diabetic nephropathy can predict response to treatment.

Condition or Disease	Intervention/Treatment	Phase
Diabetic Nephropathy	Drug: Calcitriol Drug: Placebo	Phase 4

Study Design

Study Type:

Interventional

Anticipated Enrollment :

276 participants

Allocation:

Randomized

Intervention Model:

Parallel Assignment

Masking:

Double (Participant, Investigator)

Primary Purpose:

Screening

Study Start Date :

Oct 1, 2012

Anticipated Primary Completion Date :

Apr 1, 2014

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Calcitriol Calcitriol	Drug: Calcitriol dosage of 0.5mcg administered orally once daily for 12 month
Placebo Comparator: Placebo Placebo	Drug: Placebo

Arm

Intervention/Treatment

Experimental: Calcitriol

Calcitriol

Drug: Calcitriol

dosage of 0.5mcg administered orally once daily for 12 month

Placebo Comparator: Placebo

Placebo

Drug: Placebo

Outcome Measures

Primary Outcome Measures

Changes in renal function with proteinuria [12 month after administration]
Comparison of in GFR level from baseline Comparison of proteinuria amount checked by random urine protein/creatinine ratio

Secondary Outcome Measures

changes in sTNFR and TNF-related proteins [12 months after administration]
Comparison of serum TNFR1, TNFR2 levels from baseline

Eligibility Criteria

Criteria

Ages Eligible for Study:

19 Years to 80 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

patients age 19-80 years
Clinically proven diabetic nephropathy
MDRD eGFR >= 30mL/min/1.73m2
Patients with residual urine protein/creatinine ratio >= 200mg/g
Adequate blood pressure control as treated systolic blood pressure <=140 or diastolic <=90 mmHg with RAS inhibitor for more than 3months
Serum intact PTH <500 mg/dL
Serum calcium <10.2 mg/dL
Patients who have not been treated vitamin D within the 3months prior to signing the informed consent form

Exclusion Criteria:

Patients age <19 years or > 80years
Patients with rapidly progressive glomerulonephritis
Patients requiring renal replacement therapy immediately
Hypercalcemia(Uncorrected serum calcium level >10.2 mg/dL) within recent 3month
Malignant hypertension
Heart failure (New York Heart Association functional class II to IV or LVEF <40%)
Severe chronic obstructive lung disease
Decompensated liver disease (ALT >3X upper normal limit)
Known allergy or hypersensitivity to vitamin D
Current treatment with steroids and/or immunosuppressive agents
Active primary malignancy requiring treatment or survival limits less than 2years
History of noncompliance to medical regimen
Inability to give an informed consent or to cooperate with researchers