Renal Failure Clinical Trial
— WAKOfficial title:
Preliminary Study to Assess the Safety and Efficacy of a Wearable Artificial Kidney Device for the Treatment of Patients With Endstage Renal Failure
This is a pilot study of a wearable type of kidney dialysis machine to treat patients with chronic kidney disease.
Status | Completed |
Enrollment | 8 |
Est. completion date | March 2007 |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years to 75 Years |
Eligibility |
Inclusion Criteria: - End stage renal failure - Regular haemodialysis - Cardiovascular stability - Stable vascular access Exclusion Criteria: - Allergy to heparin or ethylene oxide - Recent cardiovascular or neurological event - Unable to provide informed consent - Age < 18 |
Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
United Kingdom | UCL Center for Nephrology | London |
Lead Sponsor | Collaborator |
---|---|
Royal Free Hampstead NHS Trust | Xcorporeal |
United Kingdom,
Gura V, Beizai M, Ezon C, Polaschegg HD. Continuous renal replacement therapy for end-stage renal disease. The wearable artificial kidney (WAK). Contrib Nephrol. 2005;149:325-33. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | urea, potassium, phosphate and B2M clearances | |||
Primary | safety - cardiovascular,no hemolysis, bleeding, infection | |||
Primary | no ammonia generation from sorbents, control of acid base balance | |||
Secondary | fluid removal | |||
Secondary | patient satisfaction questionnaire | |||
Secondary | affect of treatment of cytokines |
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