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Clinical study of video assisted ultrasound guided puncture device

Clinical study of video assisted ultrasound guided puncture device

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300070446
Enrollment
Unknown
Registered
2023-04-12
Start date
2023-04-13
Completion date
Unknown
Last updated
2024-01-14

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

Conditions

None listed

Interventions

Experimental group 1:Video-assisted ultrasound-guided in-plane radial artery cannulation
Experimental group 2:Video-assisted ultrasound-guided out-plane radial artery cannulation
Experimental group 3:Video-assisted ultrasound-guided brachial plexus block
Control group 1:Traditional ultrasound-guided in-plane radial artery cannulation
Control group 2:Traditional ultrasound-guided out-plane radial artery cannulation
Control group 3:Traditional ultrasound-guided brachial plexus block

Sponsors

Department of Anesthesiology, the Second Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangdong Provincial Hospital of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 84 Years

Inclusion criteria

Inclusion criteria: 1. Radial artery group: (1) ASA Grade I to III, aged >= 18 years and = 18 years and < 85 years, no gender limit; (2) patients who accepting elective surgery requires brachial plexus block anesthesia through intermuscular sulci approach.

Exclusion criteria

Exclusion criteria: 1. Radial artery puncture group: (1) Allen test positive, emergency surgery and hand/wrist surgery, hemorrhagic shock, alternate pulse, water rush, odd pulse due to other diseases, puncture site infection, coagulopathy, or Raynaud's disease; (2) Patients who had received arterial puncture within 1 month prior to the start of the trial. 2. Brachial plexus block group: patients with coagulopathy, emergency surgery, hemorrhagic shock, and puncture site infection.

Design outcomes

Primary

MeasureTime frame
the success rate of radial artery cannulation on the first attempt;success rate of neuroblockage;nerve block procedure time;

Secondary

MeasureTime frame
procedure time;the total time to successful cannulation;the number of attempts;the number of needle redirections;the number of puncture sites;use of the transfixion technique;Use of another artery;the number of operators' head movements during the location and cannulation;complication of cannulation;the angle between the needle and the guide line;evaluated with a visual analogue scale ;onset time and duration;dose of local anesthetics;nerve stimulation;adverse events;the number of operators' head movements when never block;block performance time;postoperative VAS scores;VAS scores at rest at 6h after surgery;the angle between the needle and the midline;discomfort experienced by the patients;the anesthesiologists’ confidence as to whether their block would be successful or not;operator satisfaction score;

Countries

China

Contacts

Public ContactZhao Yue

Guangdong Provincial Hospital of Chinese Medicine

zhaoyue0489@126.com+86 186 2057 6204

Outcome results

None listed

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