Perioperatief behoud van de globale weefselperfusie en volemische status tijdens abdominale chirurgie: Nexfin hartminuutvolume en pulse pressure variatie versus arteriële bloeddruk-gestuurde therapie.
Completed
- Conditions
- Patients undergoing abdominal surgery
- Registration Number
- NL-OMON26570
- Lead Sponsor
- VU University Medical CenterWestfries Gasthuis Hoorn
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 250
Inclusion Criteria
1. Patients undergoing elective abdominal surgery;
2. Age 18-85 years;
Exclusion Criteria
1. Preexisting cardiac arrhythmias;
2. Emergency operation;
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary endpoint is defined as postoperative morbidity based on the incidence of a number of predefined complications until 7 days after surgery. These parameters include, among others, reoperation, infections, rehabilitation and restoration of gastrointestinal function.
- Secondary Outcome Measures
Name Time Method Secondary endpoints include hospital length of stay and microcirculatory perfusion.