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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03929887
Other study ID # KORNERSTONE
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date May 1, 2019
Est. completion date December 31, 2028

Study information

Verified date February 2020
Source Seoul National University Hospital
Contact Yong Chul Kim, MD,PhD.
Phone +82-10-8874-7429
Email imyongkim@gmail.com
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Glomerulonephritis (GN) generates an enormous individual and social economic burden. However, the therapeutic options are largely based on clinical and pathological parameters and the individual response to therapy or prognosis is uncertain.

Recently, along with advances in molecular analysis and computational bioinformatics, genomic data from human renal biopsies could provide a strong foundation for the future of precision medicine in nephrology.

In response to a request for applications by the Ministry of Health and Welfare of Korea for the creation of Clinical Research Registry, multi-center N network has been established for prospective cohort with kidney biopsy samples (KORNERSTONE).

Through this Network the investigators hope to understand the fundamental biology of glomerulonephritis and aim to bank long-term observational data and corresponding biological data including genomic data from kidney tissues, and kidney pathologic data which is digitalized This database is archived to a web-based platform to access easily and further enrich for researchers.


Description:

Glomerulonephritis (GN) such as Minimal change disease (MCD), focal segmental glomerulosclerosis (FSGS), Membranous nephropathy (MN), and Immunoglobulin A nephropathy (IgAN) has quite a common clinical presentation often results in renal insufficiency which generates an enormous individual and social economic burden.

However, the therapeutic options are largely based on clinical and pathological parameters and the individual response to therapy or prognosis is uncertain.

Recently, along with advances in molecular analysis and computational bioinformatics, genomic data from human renal biopsies could provide a strong foundation for the future of precision medicine in nephrology.

In response to a request for applications by the Ministry of Health and Welfare of Korea for the creation of Clinical Research Registry, a number of universities joined together to establish Korean Kidney Biopsy Network (KORNERSTONE).

Through this Network the investigators hope to understand the fundamental biology of glomerulonephritis and aim to bank long-term observational data and corresponding biological data including genomic data from kidney tissues, and kidney pathologic data which is digitalized This database is archived to a web-based platform to access easily and further enrich for researchers.

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1. Blood tests: CBC, Chemistry (Ca, P, Glucose, Total protein, Albumin, Uric acid), Electrolyte, Renal function (BUN, Creatinine, eGFR), Liver function (AST, ALT)

2. Immunologic blood tests: Complement 3, Complement 4, ASO, RF, Cryoglobulin, dsDNA, ANA

3. Urine tests: Urinalysis, Urine protein, Urine albumin, Urine creatinine

4. Radiologic tests: Kidney USG, Abdominal-pelvis computed tomography

5. Pathologic results

6. Treatment informations: treatment status, drug type, treatment duration

7. Quality of life questionnaire: Kidney Disease and Quality of Life Short Form survey (adults), PedsQL 4.0 Generic Core Scales (pediatrics)

8. Dietary questionnaire


Recruitment information / eligibility

Status Recruiting
Enrollment 3000
Est. completion date December 31, 2028
Est. primary completion date December 31, 2028
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility 1. Inclusion criteria

- Patient suspected of glomerular disease who received kidney biopsy in participating university medical centers

- Children (age<18 years) also included

2. Exclusion criteria - Patients who previously received a kidney transplant

Study Design


Intervention

Other:
Kidney Biopsy
Patients scheduled to undergo a clinically indicated kidney biopsy will be requested to consent to an additional renal core and various patient-derived samples.

Locations

Country Name City State
Korea, Republic of KangWon National University Hospital Chuncheon
Korea, Republic of Keimyung University Dongsan Medical Center Daegu
Korea, Republic of Chung-Ang University Hosptial Seoul
Korea, Republic of Seoul National University Hospital Seoul
Korea, Republic of Severance Hospital Seoul
Korea, Republic of SMG-SNU Boramae Medical Center Seoul

Sponsors (8)

Lead Sponsor Collaborator
Seoul National University Hospital Chung-Ang University Hosptial, Chung-Ang University College of Medicine, KangWon National University Hospital, Keimyung University Dongsan Medical Center, Ministry of Health & Welfare, Korea, Seoul National University Bundang Hospital, Severance Hospital, SMG-SNU Boramae Medical Center

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Death Documentation of death from any cause 60 months
Primary Deterioration of renal outcomes Doubling of serum creatinine compared to baseline serum creatinine
30% decline in follow-up estimated GFR (using the MDRD equation and/or the CKD-EPI equation) compared to baseline measurement
End stage renal disease defined as estimated GFR =10cc/min, initiation of maintenance dialysis or kidney transplantation.
60 months
Primary Improvement of clinical outcomes Remission of glomerulonephritis and proteinuria <0.3g/day (pateint who have proteinuria<0.3g/day at baseline have no improvement in clinical outcomes) 60 months
Secondary Malignancies Any cancer diagnosis of the skin, hematopoietic system, or solid organ after enrollment 60 months
Secondary Infections, Serious and Systemic Documented infection of any vital organ requiring the use of parenteral and/or oral antibiotics. 60 months
Secondary Acute Kidney Injury Documented diagnosis of acute kidney injury as defined by the RIFLE criteria and/or renal failure requiring renal replacement therapy <3 months. 60 months
Secondary Hospitalization Documented hospital admission, including observation for =24 hours. 60 months
Secondary Emergency Department/ Observation Unit Visit Documented visit to an emergency department or observation unit that does not lead to hospitalization and is less than 24 hours. 60 months
Secondary Cardiovascular/Cerebrovascular event Myocardial infarction; Congestive heart failure; Primary intractable serious arrhythmia; Peripheral vascular disease; Ischemic cerebrovascular accident; Hemorrhagic cerebrovascular accident; Thromboembolic event 60 months
Secondary New Onset Diabetes Diagnosis of diabetes as indicated by 1 or more of the following not present at enrollment
Documented diagnosis of diabetes in medical record
Casual (non-fasting) blood glucose > 200 mg/dL c) Fasting blood glucose > 126 mg/dL d) 2 hour glucose > 200 after oral glucose tolerance test e) chronic use (>6 mos) hypoglycemic therapy outside of pregnancy f) Hemogloblin A1C >= 6.5%
60 months
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