Determination In-vivo KUF for Diacap Pro Hemodialyser

Not Applicable

Completed

• Conditions: Renal Insufficiency,Chronic; Kidney Disease, End-Stage; Kidney Insufficiency; Kidney Failure,Chronic
• Interventions: Device: Diacap Pro High-Flux

• Registration Number: NCT02964429
• Lead Sponsor: B.Braun Avitum AG

Brief Summary

The main purpose of this study is the determination of the in-vivo ultrafiltration coefficient (in-vivo KUF) for Diacap Pro dialyzers following routine dialysis prescription in the United States.

Detailed Description

The in-vivo KUF for Diacap Pro High Flux dialysers with the surface sizes of 1.3/ 1.6/ 1.9 sqm will be determined as required by the US guideline "Guidance for the Content of Premarket Notifications for Conventional and High Permeability Hemodialyzers 1998" for comparison with the in-vitro KUF data.

Clinical data of at least 12 patients will be collected for determination of the in-vivo KUF complemented by safety-, performance-data for the removal of small and middle molecular substances and hemocompatibility data.

Study Timeline

• Study First Submitted: 2016-10-28
• Study First Submitted QC: 2016-11-11
• Study Start: 2016-11-14
• Study First Posted: 2016-11-16
• Primary Completion: 2016-12-23
• Study Completion: 2016-12-23
• Status Verified: 2017-02
• Last Update Submitted: 2017-02-06
• Last Update Posted: 2017-02-07

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 12

Inclusion Criteria

1. Written informed consent obtained from patient or parents/ guardian.
2. Subject age > 18
3. Effective blood flow 350 ml/min and dialysate flow in the range of 500 - 800 ml/min
4. On hemodialysis for a minimum of 3 months
5. Use of Cimino- or Gore-tex shunts
6. Routine dialysis-treatment for 240 min and 3 times per week
7. Documented dialysis adequacy parameter spKt/V >=1.2 that has been stable for past 3 months
8. Plan to dialyze at participating hemodialysis center for at least 3-months duration.
9. Free from any currently known unusual clotting or access problems
10. Hepatitis B surface antigen (HbsAg) negative, documented within the past 90 days or Hepatitis B surface antibody (anti-HBs) positive.
11. Anti HCV negative, documented within the past 90 days
12. Anti HIV negative, documented within the past 90 days Hematocrit (HCT) between 25 and 40% or haemoglobin (Hb) not less than 8 g/dL

Exclusion Criteria

1. Patients who are unable to tolerate an effective blood flow of 350 ml/min
2. Patients using catheter for dialysis
3. Pregnant or nursing woman. Women of childbearing potential must agree to avoid pregnancy during the study period
4. Previous plan for extended absences from the participating hemodialysis centre
5. Expected to be transplanted (living related donor) within the maximum of 3 months for the study period
6. Any serious medical conditions or disability, which in the opinion of the investigator, would interfere with treatment or assessment or preclude completion of the study

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Diacap Pro High-Flux	Diacap Pro High-Flux	1.3/ 1.6/ 1.9 sqm

Primary Outcome Measures

Name	Time	Method
Changes in Transmembrane Pressure (TMP) dependent on differerent ultrafiltration rates for calculation of the in-vivo ultrafiltration coefficient (in-vivo KUF)	For two of three dialysis sessions each week for a total study period of six weeks	UF-rates will be changed over a range starting from 600 ml/min to 1000 ml/min to 1400 ml/min to finally 1800 ml/min and resulting changes in Transmembrane Pressure (TMP) will be documented.

Secondary Outcome Measures

Name	Time	Method
Reduction rates dialyzer [%]	For two of three dialysis sessions each week for a total study period of six weeks	For urea; creatinine; phosphate; ß2-Microglobulin; Myoglobin; Retinol-Binding-Protein; alpha-1 Microglobulin and Albumin reduction rates will be calculated by using serum-levels at timepoints t=0 and t=240 min.
Complement-activation C3a and C5a [ng/ml]	For one of six dialysis sessions each two weeks for a total study period of six weeks	For complement activation C3a \[ng/ml\]; C5a \[ng/ml\] will be assessed at timepoints t=0, t=15; t=60; t=240 min.
Clearance data dialyzer [ml/min]	For one of six dialysis sessions each two weeks for a total study period of six weeks	For ß2M; Myoglobin; Retinol-Binding-Protein; alpha-1-Microglobulin; Albumin clearance data will be assessed by using serum samples pre- and post dialyzer at timepoints t=0 and t=240 min.
Total removal of proteins [mg/session]	For one of six dialysis sessions each two weeks for a total study period of six weeks	Spent dialysate will be collected during the entire dialysis treatment. Considering dialysate flow rate and ultrafiltration volume concentration of ß2-Microglobulin; Myoglobin; Retinol-Binding-Protein;alpha-1 Microglobulin; Albumin; Total Protein will be used to calculate total removal by multiplying with the effective spent dialysate volume
Complement-activation TAT III [µg/l]	For one of six dialysis sessions each two weeks for a total study period of six weeks	For complement activation TAT III \[µg/l\] will be assessed at timepoints t=0, t=15; t=60; t=240 min.
Inflammatory response Interleukin-1, Interleukin-6 and TNF-alpha [pg/ml]	For one of six dialysis sessions each two weeks for a total study period of six weeks	For inflammatory response Interleukin-1 \[pg/ml\]; Interleukin-6 \[pg/ml\]; TNF-alpha will be assessed at timepoints t=0; t=15; t=60; t=240 min
Inflammatory response CRP [mg/l]	For one of six dialysis sessions each two weeks for a total study period of six weeks	For inflammatory response CRP\[mg/l\] will be assessed at timepoints t=0; t=15; t=60; t=240 min
Incidence of Treatment-Emergent Adverse Events	November 2016 up to 2 months	Number of patients presenting adverse events will be assessed following CTCAE v4.0 grading.

Trial Locations

Locations (1)

Interní oddělení Strahov VFN; 🇨🇿 Praha, Czech Republic