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BeneVision N17 patient monitor multi parameter fusion analysis function clinical trial

BeneVision N17 patient monitor multi parameter fusion analysis function clinical trial

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100045894
Enrollment
Unknown
Registered
2021-04-27
Start date
2021-01-01
Completion date
Unknown
Last updated
2021-12-13

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

Conditions

Arrhythmia

Interventions

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Sponsors

PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Adult patients >=18 years old; 2. Patients who need ECG monitoring and one or more parameters of blood oxygen or invasive arterial pressure monitoring.

Exclusion criteria

Exclusion criteria: 1. Patients with continuous regular restlessness; 2. Patients undergoing CPR rescue; 3. Patients undergoing cardiopulmonary bypass surgery with artificial cardiopulmonary machine; 4. Patients undergoing V-A ECMO treatment; 5. Patients undergoing balloon counterpulsation therapy; 6. Patients with mental diseases; 7. Patients who the researchers think are not suitable; 8. Patients who are participating in other clinical trials.

Design outcomes

Primary

MeasureTime frame
Rate of decrease in false fatal alarm cases;Rate of false non fatal alarm cases decrease;Error suppression ratio of fatal alarm;

Secondary

MeasureTime frame
Error suppression ratio for non-fatal alarms;Incidence of adverse events;

Countries

China

Contacts

Public ContactHan Baoshi

PLA General Hospital

stonehan826@hotmail.com+86 13810837818

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026