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Effect of preload reduction through intermittend hemodialysis or continuous veno-venous hemofiltration on microcirculatory perfusion in patients with chronic kidney failure and critically ill patients

Effect of preload reduction through intermittend hemodialysis or continuous veno-venous hemofiltration on microcirculatory perfusion in patients with chronic kidney failure and critically ill patients - Fluid management and peripheral perfusion

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON34825
Enrollment
40
Registered
2010-04-13
Start date
2010-05-05
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

intensive care patienten microcirculatory perfusion renal replacement therapie

Interventions

None listed

Sponsors

Erasmus MC, Universitair Medisch Centrum Rotterdam
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: We will include two patientspopulations, firstly patients undergoing chronic intermittend renal replacement therapy in an outpatient clinic setting. Secondly we will include patients admitted to the intensive care unit who receive continuous veno-venous hemofiltration with ultrafiltration. Of both populations we will include 20 patients. Inclusion criteria for patients receiving chronic intermittend renal replacement therapy: - Age above 18 yrs - Admitted for intermittend hemodialysis.;Inclusioncriteria for patients admitted to the intensive care unit who receive continuous veno-venous hemofiltration. - Age above 18 yrs. - Clinical indication for continuous veno-venous hemofiltration with ultrafiltration

Exclusion criteria

Exclusion criteria: Exclusion criteria for patients receiving chronic intermittend renal replacement therapy: - Circumstances making it impossible to perform sublingual measurements, like bleeding of the oral cavity. - Patients who require no or only small amounts of ultrafiltration during hemodialysis. ;Exclusioncriteria for patients admitted to the intensive care unit who receive continuous veno-venous hemofiltration. - Circumstances making it impossible to perform sublingual measurements, like bleeding of the oral cavity

Design outcomes

Primary

MeasureTime frame
The main study parameter is the sublingual microcirculatory perfusion.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)