Hemodialysis Clinical Trial
— IPUF-HDOfficial title:
Initial Feasibility Pilot Study of Interdialytic Peritoneal Ultrafiltration to Manage Volume Status in Hemodialysis Patients
Sodium accumulates in the tissues of patients with kidney disease and impairs survival. Three-times weekly, standard hemodialysis alone cannot remove excess sodium efficiently. A sample of 10 chronic hemodialysis patients will undergo a 5-week, pilot, interventional study to test the efficacy of additional sodium removal in-between hemodialysis sessions, twice per week, for three weeks. Tissue sodium removal will be achieved with peritoneal dialysis after the surgical insertion of a peritoneal dialysis catheter. Tissue sodium removal will be assessed at the beginning and at the end of the study with sodium magnetic resonance imaging of a peripheral limb (leg). Patients will also undergo monitoring for symptoms and blood pressure throughout the study to assess the safety of this procedure.
Status | Recruiting |
Enrollment | 10 |
Est. completion date | December 31, 2024 |
Est. primary completion date | June 30, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria - At least one of the following: - Average per-session interdialytic weight gain = 4.0 % of their dry weight in the last month; - Inability to consistently achieve dry weight with the current treatment schedule; - Need for additional HD treatments to achieve prescribed dry weight. - Weekly HD sessions - up to three times/week - Age =18 years - Willing and able to give informed consent Exclusion Criteria - Contraindications to peritoneal dialysis - Contraindications to MRI - Uncontrolled diabetes mellitus - Active infections - Non-compliance to hemodialysis prescription - Pre-study serum sodium < 130 mmol/L |
Country | Name | City | State |
---|---|---|---|
Canada | London Health Sciences Centre | London | Ontario |
Lead Sponsor | Collaborator |
---|---|
Lawson Health Research Institute | Sequana Medical N.V. |
Canada,
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* Note: There are 21 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Skin sodium concentration | Skin sodium concentration at the end of week 4 as measured by sodium-23 magnetic resonance imaging of the leg. | End of week 4 | |
Primary | Adverse events | Completion of the iPUF treatment without adverse events | iPUF interventions on Week 2, 3 and 4 | |
Secondary | Interdialytic weight gain | Difference in interdialytic weight gain at run-in week vs end of intervention, vs wash-out | week 1 vs 4, week 1 vs 5-6 | |
Secondary | Total weekly sodium removal with interdialytic peritoneal ultrafiltration | Total weekly sodium removal with peritoneal dialysis in intervention weeks | week 2, 3, 4 | |
Secondary | Total volume of fluid removed with interdialytic peritoneal ultrafiltration | Total volume of fluid removed with peritoneal dialysis in intervention weeks | week 2, 3, 4 | |
Secondary | Home blood pressure | Changes in home blood pressure at baseline vs end of intervention and vs washout | week 1 vs week 4, week 1 vs 5-6 | |
Secondary | Mean intradialytic hemodynamics | Changes in mean intradialytic hemodynamic monitor parameters, as measured with Finometer and CVInsight | week 1 vs 4, week 1 vs 6 | |
Secondary | Regional wall motion abnormalities | Changes in Regional Wall Motion Abnormalities (echocardiography) at peak-stress hemodialysis | week 1 vs 4, week 1 vs 6 | |
Secondary | Symptoms | Changes in symptoms as measured with the London Evaluation of Illness questionnaire | week 1 vs 4, week 1 vs 6 | |
Secondary | Infusion pain | Infusion pain as measured with 0-10 visual analog scale | Through study completion, average of all study treatments | |
Secondary | Changes in serum sodium | Post-iPUF change in serum sodium | Through study completion, average of all study treatments |
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