- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03820401
Dialysis Performance of Different Dialyzer Membranes Using Different Coagulation Strategies
Quantification of Dialysis Performance of Different Dialyzer Membranes With Different Coagulation Strategies, Using a Reference microCT Scanning Technique
Coagulation within the dialyzer membrane fibres is an obvious biological sign of bio-incompatibility. To avoid clotting during extracorporeal treatment, an anticoagulant is added to the circuit, resulting in an increased risk for bleeding complications.
In addition, there is evidence that a substantial number of fibers can become blocked before this is reflected in routinely observed parameters, or in termination of the dialysis session. Little is known about the impact of such subclinical clotting on dialyzer performance in terms of solute clearance.
Membrane clogging due to deposition of proteins and red blood cells on the dialysis membrane may influence both the diffusive and convective transport characteristics of the dialyzer membrane before leading to complete dialyzer clotting.
In 2018, the invesitgators described a method to objectively count the number of blocked fibres inside a dialyzer using a micro-CT scanning technique.
In the present trial, the investigators use this method to assess the resistance of the dialyzer to clotting, and to evaluate the impact of subclinical fibre blocking on solute removal and thus performance of a dialyzer during a dialysis session.
The aim of this randomized cross-over study is to objectively quantify the performance of different dialyzer membranes: ATA™ membrane in the Solacea™ dialyzer, polysulfone membrane in the FX800 dialyzer, and the heparin-coated AN membrane in the Evodial dialyzer, and this with different anticoagulation strategies.
Study Overview
Status
Conditions
Detailed Description
This single centre, randomized cross-over study includes ten consecutive stable chronic hemodialysis (HD) patients who experienced stable dialysis sessions during the last 4 weeks, and had no known coagulation disorder, active inflammation or malignancy.
Double-needle vascular access is achieved through a native arterio-venous fistula or a well-functioning double lumen tunnelled central venous catheter.
In a first test series, each patient is dialyzed for 240min (at midweek) in 4 different regimens, randomly using 2 different dialyzers and 2 different anticoagulation schemes. Patients receive their regular brand of Low-Molecular-Weight Heparin anticoagulation at the beginning of the dialysis session, and this randomly either at their regular dose (full dose 1/1) or at only 50% of their regular dose (half dose 1/2). All test sessions are performed with blood flow at 300mL/min and dialysate flow at 500mL/min in post dilution hemodiafiltration (HDF) mode (substitution flow 75mL/min). Ultrafiltration rates is set according to the patient's interdialytic weight gain and clinical status:
- ATA™ Solacea 19H - HDF - 1/1 anticoagulation
- ATA™ Solacea 19H - HDF - 1/2 anticoagulation
- polysulfone FX800 - HDF - 1/1 anticoagulation
- polysulfone FX800 - HDF - 1/2 anticoagulation
During the 4 experimental midweek sessions, blood is sampled from the arterial and venous blood lines, and spent dialysate is sampled from the outlet line, all at 60min after the dialysis start. Blood samples are immediately centrifuged and serum and dialysate are stored at -80°C until batch analysis.
Concentrations of urea, kappa and lambda free light chains, and myoglobin are determined. Extraction ratios and adsorption on the membrane are calculated from concentrations.
At the end of the dialysis session, a standard rinsing procedure of the hemodialyzer is performed using exact 300mL rinsing solution. Next, the hemodialyzer is dried using continuous positive pressure ventilation. Dialyzer fibre blocking is visualized in the dialyzer outlet potting using a 3D CT scanning technique on micrometer resolution. HECTOR is a High Energy CT scanner Optimized for Research, built by the Ghent University Centre for X-ray Tomography (UGCT) in collaboration with the UGCT spin-off company XRE (Gent, Belgium). In front of the X-ray source, the dialyzer is mounted vertically on a precision rotation stage, and radiographies were recorded over 360° with an angular interval of 0.15°. Scan conditions are optimized to maximize the signal-to-noise ratio based on the sample size and structure, and the scanner properties. The tube voltage is set at 80kV, at a power of 20 Watts, the maximal power that allowed imaging at a resolution of 25µm. A total of 2401 projections are recorded with 500ms exposure each, resulting in a total exposure time of 20 minutes. Acquired images at 0 (projection 1) and 360° (projection 2401) are compared to exclude movement of the hemodialyzer during the scanning process. Reconstruction of the raw projection data is performed with the Octopus Reconstruction software package, licensed by XRE23.
Fibers are counted in the central cross-section of the dialyzer outlet potting in a computer-based way using the Fiji image processing toolkit of ImageJ analysis software (ImageJ 1.51H, NIH, Bethesda, USA), an open-source platform for biological-image analysis.
In a second test series in 10 stable HD patients, no blood sampling is performed but dialyzers are scanned post dialysis. The following different dialyzers in HD modus at midweek are tested:
- ATA™ Solacea 19H - HD - 1/1 anticoagulation
- ATA™ Solacea 19H - HD - 1/2 anticoagulation
- polysulfone FX800 - HD - 1/1 anticoagulation
- polysulfone FX800 - HD - 1/2 anticoagulation
- polysulfone FX800 - HD - 1/2 anticoagulation - with predialysis albmuin priming of the membrane
- Evodial - HD - no anticoagulation
- Evodial - HD - no anticoagulation - with predialysis albmuin priming of the membrane
In a third test series in 10 stable HD patients, no blood sampling is performed but dialyzers are scanned post dialysis. The following different dialyzers at midweek are tested:
- ATA™ Solacea 19H - pre dilution HDF (substitution 150mL/min) - 1/4 anticoagulation
- ATA™ Solacea 19H - post dilution HDF (substitution 75mL/min) - 1/4 anticoagulation
- ATA™ Solacea 19H - HD - 1/4 anticoagulation
- ATA™ Solacea 19H - pre dilution HDF (substitution 150mL/min) - no anticoagulation
- ATA™ Solacea 19H - post dilution HDF (substitution 75mL/min) - no anticoagulation
- ATA™ Solacea 19H - HD - no anticoagulation
First outcome measure: relative number of open fibers in each tested dialyzer. Second outcome measure: dialyzer performance (extraction ratio, adsorption).
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Gent, Belgium
- Ghent University Hospital - Nephrology
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- 18 years or older
- experienced stable dialysis sessions during the last 4 weeks
- double needle/lumen well-functioning vascular access
Exclusion Criteria:
- known coagulation disorder
- active inflammation
- malignancy
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Solacea_postHDF_1/1anticoagulation
intervention:
measurements:
|
Fiber blocking is calculated in different commercially available dialyzers
Fiber blocking is calculated in different commercially available dialyzers used in different dialysis stategies
Fiber blocking is calculated in different commercially available dialyzers using different anticoagulation strategies
|
|
Experimental: Solacea_postHDF_1/2anticoagulation
intervention:
measurements:
|
Fiber blocking is calculated in different commercially available dialyzers
Fiber blocking is calculated in different commercially available dialyzers used in different dialysis stategies
Fiber blocking is calculated in different commercially available dialyzers using different anticoagulation strategies
|
|
Experimental: FX800_postHDF_1/1anticoagulation
intervention:
measurements:
|
Fiber blocking is calculated in different commercially available dialyzers
Fiber blocking is calculated in different commercially available dialyzers used in different dialysis stategies
Fiber blocking is calculated in different commercially available dialyzers using different anticoagulation strategies
|
|
Experimental: FX800_postHDF_1/2anticoagulation
intervention:
measurements:
|
Fiber blocking is calculated in different commercially available dialyzers
Fiber blocking is calculated in different commercially available dialyzers used in different dialysis stategies
Fiber blocking is calculated in different commercially available dialyzers using different anticoagulation strategies
|
|
Experimental: Solacea_HD_1/1anticoagulation
intervention:
measurement: - microCT scanning of rinsed and dried dialyzer, post dialysis in order to count open fibers |
Fiber blocking is calculated in different commercially available dialyzers
Fiber blocking is calculated in different commercially available dialyzers used in different dialysis stategies
Fiber blocking is calculated in different commercially available dialyzers using different anticoagulation strategies
|
|
Experimental: Solacea_HD_1/2anticoagulation
intervention:
measurements: - microCT scanning of rinsed and dried dialyzer, post dialysis in order to count open fibers |
Fiber blocking is calculated in different commercially available dialyzers
Fiber blocking is calculated in different commercially available dialyzers used in different dialysis stategies
Fiber blocking is calculated in different commercially available dialyzers using different anticoagulation strategies
|
|
Experimental: FX800_HD_1/1anticoagulation
intervention:
measurements: - microCT scanning of rinsed and dried dialyzer, post dialysis in order to count open fibers |
Fiber blocking is calculated in different commercially available dialyzers
Fiber blocking is calculated in different commercially available dialyzers used in different dialysis stategies
Fiber blocking is calculated in different commercially available dialyzers using different anticoagulation strategies
|
|
Experimental: FX800_HD_1/2anticoagulation
intervention:
measurements: - microCT scanning of rinsed and dried dialyzer, post dialysis in order to count open fibers |
Fiber blocking is calculated in different commercially available dialyzers
Fiber blocking is calculated in different commercially available dialyzers used in different dialysis stategies
Fiber blocking is calculated in different commercially available dialyzers using different anticoagulation strategies
Fiber blocking is calculated in different commercially available dialyzers either preprimed with Albumin or not
|
|
Experimental: FX800_HD_1/2anticoagulation_albuprime
intervention:
measurement: - microCT scanning of rinsed and dried dialyzer, post dialysis in order to count open fibers |
Fiber blocking is calculated in different commercially available dialyzers
Fiber blocking is calculated in different commercially available dialyzers used in different dialysis stategies
Fiber blocking is calculated in different commercially available dialyzers using different anticoagulation strategies
Fiber blocking is calculated in different commercially available dialyzers either preprimed with Albumin or not
|
|
Experimental: Evodial_HD_no anticoagulation
intervention:
measurement: - microCT scanning of rinsed and dried dialyzer, post dialysis in order to count open fibers |
Fiber blocking is calculated in different commercially available dialyzers
Fiber blocking is calculated in different commercially available dialyzers used in different dialysis stategies
Fiber blocking is calculated in different commercially available dialyzers using different anticoagulation strategies
|
|
Experimental: Evodial_HD_no anticoagulation_albuprime
intervention:
measurement: - microCT scanning of rinsed and dried dialyzer, post dialysis in order to count open fibers |
Fiber blocking is calculated in different commercially available dialyzers
Fiber blocking is calculated in different commercially available dialyzers used in different dialysis stategies
Fiber blocking is calculated in different commercially available dialyzers using different anticoagulation strategies
Fiber blocking is calculated in different commercially available dialyzers either preprimed with Albumin or not
|
|
Experimental: Solacea_preHDF_1/4anticoagulation
intervention:
measurements: - microCT scanning of rinsed and dried dialyzer, post dialysis in order to count open fibers |
Fiber blocking is calculated in different commercially available dialyzers
Fiber blocking is calculated in different commercially available dialyzers used in different dialysis stategies
Fiber blocking is calculated in different commercially available dialyzers using different anticoagulation strategies
|
|
Experimental: Solacea_postHDF_1/4anticoagulation
intervention:
measurements: - microCT scanning of rinsed and dried dialyzer, post dialysis in order to count open fibers |
Fiber blocking is calculated in different commercially available dialyzers
Fiber blocking is calculated in different commercially available dialyzers used in different dialysis stategies
Fiber blocking is calculated in different commercially available dialyzers using different anticoagulation strategies
|
|
Experimental: Solacea_HD_1/4anticoagulation
intervention:
measurements:microCT scanning of rinsed and dried dialyzer, post dialysis in order to count open fibers |
Fiber blocking is calculated in different commercially available dialyzers
Fiber blocking is calculated in different commercially available dialyzers used in different dialysis stategies
Fiber blocking is calculated in different commercially available dialyzers using different anticoagulation strategies
|
|
Experimental: Solacea_preHDF_no anticoagulation
intervention:
measurements: - microCT scanning of rinsed and dried dialyzer, post dialysis in order to count open fibers |
Fiber blocking is calculated in different commercially available dialyzers
Fiber blocking is calculated in different commercially available dialyzers used in different dialysis stategies
Fiber blocking is calculated in different commercially available dialyzers using different anticoagulation strategies
|
|
Experimental: Solacea_postHDF_no anticoagulation
intervention:
measurements: - microCT scanning of rinsed and dried dialyzer, post dialysis in order to count open fibers |
Fiber blocking is calculated in different commercially available dialyzers
Fiber blocking is calculated in different commercially available dialyzers used in different dialysis stategies
Fiber blocking is calculated in different commercially available dialyzers using different anticoagulation strategies
|
|
Experimental: Solacea_HD_no anticoagulation
intervention:
measurements: - microCT scanning of rinsed and dried dialyzer, post dialysis in order to count open fibers |
Fiber blocking is calculated in different commercially available dialyzers
Fiber blocking is calculated in different commercially available dialyzers used in different dialysis stategies
Fiber blocking is calculated in different commercially available dialyzers using different anticoagulation strategies
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Number of open fibres in the dialyzer
Time Frame: 17 weeks
|
Number of open fibres as assessed post dialysis by a reference microCT scanning technique
|
17 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Extraction ratio of three middle molecules in the dialyzer
Time Frame: 4 weeks
|
Extraction ratio from myoglobin, kappa and lambda free light chains as calculated from their concentrations at the dialyzer inlet en outlet
|
4 weeks
|
Collaborators and Investigators
Sponsor
Collaborators
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- UGent_FiberClotting_1
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Hemodialysis
-
National Taiwan University HospitalCompletedHemodialysis Complication | Hemodialysis-Induced SymptomTaiwan
-
University Hospital, GhentEnrolling by invitationPediatric | Efficiency | Hemodialysis Treatment | Hemodialysis PatientBelgium
-
Khon Kaen UniversityCompletedHemodialysis | Hemodialysis Treatment | Dialysis AdequacyThailand
-
Vantive Health LLCBaxter Healthcare Corporation; Gambro Renal Products, Inc.Completed
-
Osaka UniversityCompleted
-
Chinese PLA General HospitalWithdrawn
-
University of HyogoCompleted
-
DVX, LLCNational Institute of Diabetes and Digestive and Kidney Diseases (NIDDK); Renal...Completed
-
Dong-A UniversityCompletedHemodialysisKorea, Republic of
Clinical Trials on choice of dialyzer
-
Hospital Clinic of BarcelonaFresenius Medical Care Deutschland GmbHCompleted
-
Vantive Health LLCBaxter Healthcare CorporationCompleted
-
Vantive Health LLCBaxter Healthcare CorporationCompletedEnd Stage Renal DiseaseChina
-
Kyungpook National University HospitalBaxter Healthcare Corporation; Kyungpook National University Chilgok Hospital; Yeungnam University Hospital and other collaboratorsCompletedEnd Stage Renal DiseaseKorea, Republic of
-
The University of Hong KongBaxter Healthcare CorporationCompleted
-
Vantive Health LLCBaxter Healthcare CorporationCompletedEnd Stage Renal DiseaseGermany
-
Royal Free Hampstead NHS TrustCompletedChronic Kidney DiseaseUnited Kingdom
-
Réseau de Santé Vitalité Health NetworkUnknownEnd Stage Renal Disease on DialysisCanada
-
Vantive Health LLCBaxter Healthcare CorporationCompletedEnd Stage Renal DiseaseAustria
-
Carlo Maria GuastoniUnknown