MINIMAL INVASIVE MONITORING OF VOLUME STATUS IN PATIENTS AFTER MAJOR ABDOMINAL SURGERY.

MINIMAL INVASIVE MONITORING OF VOLUME STATUS IN PATIENTS AFTER MAJOR ABDOMINAL SURGERY. - -

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON39163

Enrollment

Registered

2010-04-01

Start date

2011-02-28

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

After major abdominal surgery

Interventions

Hemodynamic measurements are performed during propofol infusion at a blood concentration of 4, 2 and 1 µg•mL-1. Subsequently measurements are repeated prior to, 30 seconds after start and 2 minutes

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - Scheduled for ventilation and sedation at the PACU after elective major abdominal surgery (i.e. any type of abdominal surgery with an indication for invasive monitoring with arterial en central venous catheters) - Aged 18-65 years. - Being able to give written informed consent prior to surgery.

Exclusion criteria

Exclusion criteria: - Pregnancy - Documented or suspected soybean protein and/or relevant drug allergy. - Morbid obesity (BMI > 35) - venous pressure (CVP) >18 mm Hg and/ or a cardiac index

Design outcomes

Primary

Measure	Time frame
Cardiac ouput measured with different pulse contour methods to measure CO compared to thermodilution CO measured with a PAC	—

Secondary

Measure	Time frame
-	—

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)