Skip to content

A Clinical Trial of Comparing the Accuracy of Non-invasive Blood Pressure Monitor with Invasive Monitor

A Clinical Trial of Comparing the Accuracy of Non-invasive Blood Pressure Monitor with Invasive Monitor

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000039668
Enrollment
Unknown
Registered
2020-11-05
Start date
2020-11-04
Completion date
Unknown
Last updated
2021-02-08

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

Conditions

None listed

Interventions

Gold Standard:Invasive arterial test results
of&#32
blood&#32
pressure&#32
(Monitor&#32
B,F,K,L,M)

Sponsors

Department of Anesthesiology, the Second Affiliated Hospital of Army Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1) Surgical patients with invasive arterial pressure monitoring according to their condition; 2) Aged 18-70 years old; 3) ASA grade I-III; 4) Patients who volunteer and sign informed consent.

Exclusion criteria

Exclusion criteria: 1) Patient's condition is unstable; 2) Patients with severe heart disease or arrhythmia; 3) Patients using cardiopulmonary machines and defibrillators; 4) Patients with vascular disease; 5) BMI = 30; 6) Pregnant woman; 7) Patients with infection, trauma, inaccessible radial artery pulsation or abnormal Allen test at the arterial puncture site; 8) Other diseases considered unsuitable for participation in this clinical trial.

Design outcomes

Primary

MeasureTime frame
blood pressure;ACC;

Countries

China

Contacts

Public ContactHong Li

The Second Affiliated Hospital of Army Medical University

472217836@qq.com+86 23-68774997

Outcome results

None listed

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