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Feasibility study of invasive blood pressure monitoring via the distal radial artery approach

Feasibility study of invasive blood pressure monitoring via the distal radial artery approach

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100043714
Enrollment
Unknown
Registered
2021-02-27
Start date
2021-05-01
Completion date
Unknown
Last updated
2021-08-30

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

Conditions

Radial artery cannulation

Interventions

Sponsors

General Hospital of Eastern Theater Command
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. The subjects who signed the written informed consent; 2. Subjects of ASA I-III; 3. Subjects older than or equal to 18 years old.

Exclusion criteria

Exclusion criteria: 1. Patients with pulseless in distal radial artery or forearm radial artery; 2. Patients with mental illness, hearing impairment, etc; 3. Patients with puncture site infection; 4. Patients who need operation or injury at puncture site; 5. Patients with peripheral vascular diseases; 6. Patients with negative Allen test; 7. Patients with coagulation dysfunction; 8. Patients participating in other clinical trials; 9. The sponsor or researcher or their family members directly involved in the trial; 10. Patients that the researchers believe cannot be included for any reason.

Design outcomes

Primary

MeasureTime frame
First-attempt Success Rate;

Secondary

MeasureTime frame
diameter, depth and cross-sectional area of artery;artery cannulation time;postoperative compression time;posterior arterial wall puncture;Abnormal blood pressure waveform during operation;complications;

Countries

China

Contacts

Public ContactDuan manlin

General Hospital of Eastern Theater Command

dml9001@163.com+86 25-80863147

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 19, 2026