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Perioperative validation of the non-invasive hemodynamic measuring device TL-400

Perioperative validation of the non-invasive hemodynamic measuring device TL-400

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON26680
Enrollment
20
Registered
2016-12-02
Start date
2017-01-01
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

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

Interventions

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.

Sponsors

Radboud university medical centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All patients receiving invasive hemodynamic monitoring as standard perioperative monitoring are eligible for inclusion. Age > 18 years

Exclusion criteria

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 outcomes

Primary

MeasureTime frame
Cardiac output, systolic blood pressure, diastolic blood pressure, mean blood pressure, stroke volume

Contacts

Public ContactL. Baggen

Radboud university medical centre, Department of Anaesthesia, pain and palliative care medicine

Lonneke.Baggen@radboudumc.nl+31(0)243614406

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)