Chronic Kidney Failure
Conditions
Keywords
Chronic kidney failure, Heparin, Hemodialysis, Biocompatibility
Brief summary
The current clinical study aims at defining an index of Anti Xa, which is the marker to evaluate the activity of heparin, at the end of the dialysis treatment and so showing the possibility to decrease heparin doses during hemodialysis when using Evodial hemodialyzer. Actually, an elevated value of AntiXa at the end of the dialysis treatment increases the risk of bleeding for patients with diabetic retinopathy, or for instance in case of fall at home.
Detailed description
In parallel to the new hemodialyzer, Evodia blood lines were developed to improve characteristics of the extracorporeal circuit in term of reduced activation of the coagulation system and lower deposits of clot components. The aim is to provide a system (hemodialyzer and extracorporeal circuit) with a low thrombogenicity and that can be used with low heparin dose in order to reduce the patients' bleeding risk at the end of HD treatment. Measurements of TAT (Thrombin-Antithrombin), the marker of the activation of the coagulation, will be performed during the study in order to evaluate the thrombogenicity of the system. The ionic clearance will be collected during all treatments to evaluate the performance of the hemodialyzer. The study will be divided into three steps * Period 1: Usual heparin dose with usual hemodialyzer and standard blood lines (baseline), * Period 2: Decrease of heparin dose with Evodial hemodialyzer and standard bloodlines * Period 3: Lowest heparin dose defined in step 2 using the system Evodial hemodialyzer and SMA bloodlines. Each patient included into the study will perform the three steps. As the risk of extracorporeal circuit clotting will be rather important, no control group (usual hemodialyzer with heparin decrease dose) will be performed.
Interventions
DEVICEEvodial hemodialysers and Evodia blood lines
Maximum 8 weeks treatment with Evodial dialysers with reduction of heparin dose
Sponsors
Gambro Lundia AB
Baxter Healthcare Corporation
Vantive Health LLC
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Patients suffering from chronic renal failure, * Patients treated in HD three times a week for at least 3 months, with a stable heparin dose and the same filter, * Patients treated in 4-4.5 hours HD mode with a blood flow between 300-350 ml/min, * Patients for whom either LMWH (Enoxaparin, Nadroparin, Tinzaparin) or UFH is used, * Patients with a well-functioning vascular access as judged by the investigator, * Patients treated either on AK, Innova or Integra dialysis machines equipped with ionic dialysance device, * Patients older than 18 years, * Patients with negative serologies (AIDS, Hepatitis) * Patients having signed consent to participate in the study.
Exclusion criteria
* Patient with HIT or known heparin allergy, * Patient treated in HD in single needle mode, * Patients with catheter, * Patients with acute inflammatory event that may affect, as judged by investigator patients' safety or study results, * Patients participating in other studies that could interfere with the objective of this study, * Patients with active malignant disease, * Patients receiving heparin outside dialysis treatment, * Patients under guardianship, * Pregnant women, nursing mothers and women planning a pregnancy during the course of this study, * Patients with serious history of coagulopathy, * Patients receiving Anti-Vitamin K medication, * Patients receiving an association of anti platelets agents, * Patients with heparin dose that can not be reduced for technical reason (excluding patients receiving too low heparin dose with no possibility of further reduction).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary criterion is the measurement of Anti Xa at the end of dialysis sessions. | End of dialysis treatment |
Secondary
| Measure | Time frame |
|---|---|
| Follow-up of aPTT for patients treated with UFH, | Kinetic on single dialysis treatment |
| Evaluation of TAT (Thrombin-Antithrombin) complex, | Kinetic on single dialysis treatment |
| Follow-up of ionic clearance (Diascan) measurements during HD sessions, | Kinetic of single dialysis treatment |
| Evaluation of the quality of the rinse-back (filter and circuit) via a visual scale, | End of dialysis treatment |
| Follow-up of AE/SAE. | All treatments during study period |
Countries
France, Germany, Italy, Sweden
Outcome results
None listed