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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04211571
Other study ID # KNU-Theranova-01
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 23, 2020
Est. completion date September 24, 2023

Study information

Verified date November 2023
Source Kyungpook National University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Theranova is a novel medium cut-off dialyzer and has better performance for removal of middle molecules compared to conventional hemodialysis. The study investigates the effect of Theranova dialzyer on preserving residual renal function in the incident hemodialysis pateitns compared to high-flux dialzyer. The primary endpoint is change of glomerular filtration rate, calculated using creatinine and urea clearance. The secondary endpoints are serial changes of glomerular filtration rate and daily urine volume, changes of serum middle molecule concentrations, hospitalization, mortality, and patient reported outcomes.


Recruitment information / eligibility

Status Completed
Enrollment 80
Est. completion date September 24, 2023
Est. primary completion date September 17, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Incident end-stage renal disease ESRD patient receiving hemodialysis for less than 1 month - 18 years old and older - Creatinine clearance of more than 2 ml/min - Agreement to participate in the clinical study - Vascular access by arteriovenous fistula/graft Exclusion Criteria: - Plan for kidney transplantation within 6 months - Severe volume overloading state - Dialysis through permanent catheter - Any hematologic malignancy or monoclonal gammopathy - Any malignancy - Active infectious disease - HIV infection - Patient enrolled to another study within 3 month from starting the present study

Study Design


Intervention

Device:
Theranova 400 dialyzer
Hemodialysis using Theranova 400 dialyzer
High-flux dialyzer
Hemodialysis using high-flux dialyzer

Locations

Country Name City State
Korea, Republic of Kyungpook national university chilgok hospital Daegu

Sponsors (5)

Lead Sponsor Collaborator
Kyungpook National University Hospital Baxter Healthcare Corporation, Ewha Womans University, Kyungpook National University Chilgok Hospital, Yeungnam University Hospital

Country where clinical trial is conducted

Korea, Republic of, 

References & Publications (1)

Kirsch AH, Lyko R, Nilsson LG, Beck W, Amdahl M, Lechner P, Schneider A, Wanner C, Rosenkranz AR, Krieter DH. Performance of hemodialysis with novel medium cut-off dialyzers. Nephrol Dial Transplant. 2017 Jan 1;32(1):165-172. doi: 10.1093/ndt/gfw310. Erratum In: Nephrol Dial Transplant. 2021 Jul 23;36(8):1555-1556. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Change of glomerular filtration rate Glomerular filtration rate is calculated as the mean of creatinine and urea clearance adjusted for body surface area. The outcome refers to the mean difference of glomerular filtration rate between baseline and after 12 months. Between baseline and 12 months
Secondary Change of glomerular filtration rate Calculated as the mean of creatinine and urea clearance adjusted for body surface area 0, 3, 6, 9, 12 months
Secondary Change of daily urine volume Total urine output for 24 hours 0, 3, 6, 9, 12 months
Secondary Change and reduction ratio of inflammatory marker levels TNF-alpha, GDF-15, etc. 0, 12 months
Secondary Change of hs-CRP hs-CRP 0, 12 months
Secondary Change of Beta 2-microglobulin Beta 2-microglobulin 0, 12 months
Secondary Change of kidney injury markers NGAL, KIM-1, TIMP-2, IGFBP-7, etc 0, 12 months
Secondary Change of cystatin-C Cystatin-C 0, 12 months
Secondary Change and reduction ratio of Kappa and lambda free light chains Kappa and lambda free light chains 0, 12 months
Secondary Hospitalization Frequency, cause, etc. Through 12-month study duration
Secondary Mortality Deaths number and causes of death Through 12-month study duration
Secondary Patient-reported outcome Using Kidney Disease Quality of Life Questionnaire-36™ (KDQOL-36™; score ranges from 0 to 100 - higher scores represent better quality of life) 0, 12 months
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