None listed
Conditions
Interventions
Sponsors
None listed
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients treated by HD 2 or 3 times a week, for at least 2 months; 2. Patients able to understand the study procedures; 3. Patients willing to provide written informed consent.
Exclusion criteria
Exclusion criteria: 1. Current age younger than 18 years treatment by HDF or high flux HD in the preceding 6 months; 2. Severe incompliance life expectancy < 3 months due to non renal disease; 3. Participation to other clinical intervention trials evaluating cardiovascular outcome.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Cardiovascular morbidity and mortality. This is a composite endpoint comprising fatal and non-fatal myocardial infarction and stroke, and vascular death (death due to vascular disease). Also all-cause mortality is considered a primary endpoint. | — |
Secondary
| Measure | Time frame |
|---|---|
| Changes in carotid intima media thickness (cIMT), aortic pulse wave velocity (PWV), left ventricular mass index (LVMi), interdialytic blood pressure, laboratory assessments (oxidative stress; acute phase response; lipid profile; various), quality of life, and nutritional state. | — |
Contacts
University Medical Center Utrecht (UMCU), Department of Nephrology, Room F03.226, P.O. Box 85500