CNAP™ Monitor Study

Accuracy of the CNAP™ Monitor in Providing Beat-to-beat Non-invasive Blood Pressure Readings

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01356082

Enrollment

Registered

2011-05-19

Start date

2011-05-31

Completion date

2012-04-30

Last updated

2012-05-02

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

Conditions

Cardiac Surgery, Spinal Surgery

Brief summary

A newly developed monitor for continuous non-invasive blood pressure monitoring (CNAP™ Monitor 500; CNSystems Medizintechnik AG, Graz, Austria) provides beat-to-beat BP readings and is non-invasive. To make sure that anaesthesiologist can rely on and make clinical decisions based on values provided by the CNAP™ monitor, to demonstrate its reliability we will test it during the perioperative care of children.

Interventions

DEVICECNAP

Non-invasive blood pressure monitor

Study design

Observational model

CASE_ONLY

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

5 Years to 18 Years

Healthy volunteers

Inclusion criteria

* Patients who will already be having an indwelling arterial cannula placed for their surgical procedure.

Exclusion criteria

* Patients with history of a peripheral neurologic or neuropathic disorder. * Patients in whom an invasive arterial cannula cannot be placed. * Patients with vascular implants at the sites of non-invasive blood pressure measurement (fingers and upper arm of the examined arm). * Edematous patients. * Patients who are less than 20 kg.

Design outcomes

Primary

Measure	Time frame
Blood pressure	1 Day (day of surgery)

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026