FindTrial
Sign In

Continuous, on-line determination of the plasma refill rate during combined hemodialysis and ultrafiltration

Continuous, on-line determination of the plasma refill rate during combined hemodialysis and ultrafiltration - COPR

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON31569
Enrollment
20
Registered
2008-02-12
Start date
2008-03-27
Completion date
Unknown
Last updated
2024-08-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

chronic renal failure

Interventions

The patients are compared under different ultrafiltration conditions (part A). Next, the target dry weight is determined (using primary study parameters), and the patients are ultrafiltrated accordi

Sponsors

Universitair Medisch Centrum Utrecht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Hemodialysis

Exclusion criteria

Exclusion criteria: Onvermogen om informed consent te geven.

Design outcomes

Primary

MeasureTime frame
Hydration status determined by: natriuretic peptides (BNP) before and after dialysis, blood volume monitoring, blood pressure and heart frequency during dialysis, non-invasive measuring of the extracellulair volume using bioimpedance analysis, ultrasonography of the vena cava one hour after dialysis, chest X-ray and 24-hour blood pressure measurement one day after dialysis (=part B, implementation).—

Secondary

MeasureTime frame
Refill in the BV target range (=part A, methodology).—

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)