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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04705506
Other study ID # 186/60
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 5, 2017
Est. completion date March 1, 2019

Study information

Verified date January 2021
Source Bangkok Metropolitan Administration Medical College and Vajira Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Dipeptidyl peptidase-4 (DPP-4) inhibitors improve glycemic control and contain pleiotropic actions on kidney injury, albuminuria and vascular inflammation especially in animal models. We plan to evaluate the efficacy of potent DPP4-inhibitors (gemigliptin) in response to these aspects in diabetic nephropathy patients.


Description:

This is a multi-center, prospective, randomized, placebo-controlled trial. A total of 201 participants were enrolled and randomly assigned to gemigliptin 50 mg daily and standard care of diabetes mellitus for 6 months. The changes of coronary calcium score (CAC score), cardio-ankle vascular index (CAVI), estimated glomerular filtration rate (GFR), markers of vascular calcification and markers of tubular renal injury were evaluated at baseline and 6 months.


Recruitment information / eligibility

Status Completed
Enrollment 201
Est. completion date March 1, 2019
Est. primary completion date March 1, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - Patients with CKD stage 1-3 (eGFR 15-60 ml/min/1.73mL) - Non-insulin dependent diabetes mellitus , blood glucose level 30-250 mg/dL - Had clinical features compatible with diabetic nephropathy (urine micro albuminuria > 30 g/g creatinine or has evidence of diabetic retinopathy Exclusion Criteria: - History of allergy to DPP4-inhibitor - Concurrent infectious disease - Inflammatory diseases - Post kidney transplantation - Receiving cinacalcet, bisphosphonate ,previously treated with DPP4-Inhibitors and sodium-glucose cotransporter-2 inhibitor (SGLT2-i).

Study Design


Intervention

Drug:
Gemigliptin
We collected baseline data from all participants for demographic characteristics,comorbid conditions and biochemistry indexes.The biomarkers for vascular calcification and renal injury were collected.Baseline CAC score and CAVI were done.The patients then were randomized into 2 groups: Group 1 received gemigliptin 50 mg /day for 6 months in addition to standard treatment ,Group 2 will have standard treatment for diabetes mellitus (DM) and chronic kidney disease (CKD).The patients will be followed up every eight weeks.Fasting plasma glucose ,BUN creatinine and 24 hour urine protein were measured at each study visit.Patients were scheduled for follow-up visits at months 2,4,and 6.After 6 months ,all the blood tests,CAC score and CAVI will be done again.

Locations

Country Name City State
Thailand 2 Division of Nephrology,Department of Medicine Pramongkutklao Hospital and College of Medicine,Thailand Bangkok
Thailand Department of Medicine,Police General Hospital,Thailand Bangkok
Thailand Faculty of Medicine ,Vajira Hospital Bangkok

Sponsors (1)

Lead Sponsor Collaborator
Bangkok Metropolitan Administration Medical College and Vajira Hospital

Country where clinical trial is conducted

Thailand, 

Outcome

Type Measure Description Time frame Safety issue
Primary Markers of renal injury urine NGAL/Cr,urine Kim-1/Cr,urine LFABP/Cr (pg/mL) 6 months
Primary Markers of vascular calcification serum bone alkaline phosphatase(pg/mL),osteopontin (pg/mL) 6 months
Primary Markers of renal injury Protienuria (mg/day) 6 months
Primary Markers of renal injury eGFR (mL/min/1.73m2) 6 months
Primary Markers of vascular calcification Reactive oxygen species (ng/mL) 6 months
Primary Markers of vascular calcification CAVI,CAC score(unit) ,CAVI normal less than8 ,CAC score normal less than 100 6 months
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