No registrations found.
ID
Source
Health condition
hemodynamic changes, low blood pressure, fluid challenge, vasopressant/inotropic agent administration, measurement cardiac output, measurement blood pressure, non invasive cardiac output measurement. hemodynamische veranderingen , vocht bolus, cardiac output meting, bloeddruk meting, non invasieve cardiac output meting
Sponsors and support
Intervention
Outcome measures
Primary outcome
Cardiac output, systolic blood pressure, diastolic blood pressure, mean blood pressure, stroke volume
Secondary outcome
none
Background summary
Perioperative validation study to compare TL-400 hemodynamic device with the standard PiCCO measuring device by comparing simultaneous CO and BP measurements at predetermined time points
Study objective
Are hemodynamic values obtained by the non invasive hemodynamic measuring device TL-400 comparable with the values obtained by the standard invasive hemodynamic measuring devices (transpulmonary thermodilution (TPTD) (PiCCO system; Pulsion Medical Systems) or pulmonary artery catheter (PAC)
Study design
Simultaneous CO and BP measurements were performed at seven predetermined time points (T1-T7): after induction of general anaesthesia but before surgical incision (T1), 30 minutes after start CRS (T2), 30 minutes before end of CRS or halfway iv chemotherapy (T3), after CRS and before the start HIPEC procedure (T4), halfway through HIPEC (T5), after the end of chemotherapy perfusion (T6), end of surgery (T7)
Intervention
After insertion of the standard invasive measuring device, the TL 400 sensor is placed around the wrist at the point where the radial artery is palpable over the head of the os radius.
L. Baggen
Geert-Grooteplein-zuid 10 (route 715), Postbus 9101
Nijmegen 6500 HB
The Netherlands
+31(0)243614406
Lonneke.Baggen@radboudumc.nl
L. Baggen
Geert-Grooteplein-zuid 10 (route 715), Postbus 9101
Nijmegen 6500 HB
The Netherlands
+31(0)243614406
Lonneke.Baggen@radboudumc.nl
Inclusion criteria
All patients receiving invasive hemodynamic monitoring as standard perioperative monitoring are eligible for inclusion.
Age > 18 years
Exclusion criteria
Severe peripheral vascular disease
Severe tricuspid or aortic valve regurgitation
Anatomical abnormalities at the wrist so the TL-400 brace cannot be applied.
Refusal of the patient
Design
Recruitment
IPD sharing statement
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
| Register | ID |
|---|---|
| NTR-new | NL6812 |
| NTR-old | NTR6998 |
| Other | METC RadboudUMC : 2017-3203 |