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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03920423
Other study ID # 1338
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 22, 2019
Est. completion date January 17, 2020

Study information

Verified date August 2020
Source Peking Union Medical College Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study is designed to evaluate and validate impact factors to success and complication using ultrasound guided short-axis out-of-plane dynamic approach, and validate the impaction.


Description:

The study including two phase: observational phase and validation phase. In observational phase, factors relative to success catheterization without posterior puncture and success in first attempt are evaluated. In validation phase, patients are randomized into different depth group with or without injection of saline. Success without posterior wall puncture, success in first attempt and overall, catheterization time are compared between groups.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date January 17, 2020
Est. primary completion date January 17, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- requirement of radial arterial catheterization during perioperative period

- within cardiac-vascular disease

- written consent

Exclusion Criteria:

- contraindication to radial arterial catheterization

- abnormal artery evaluated by ultrasonography

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
improvement of arterial depth
deepen radial arterial depth by injection of saline to more than deep cutoff point relative to result.

Locations

Country Name City State
China Peking Union Medical College Hospital Beijing

Sponsors (1)

Lead Sponsor Collaborator
Peking Union Medical College Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary success without posterior wall puncture success to puncture and catheterize of radial artery, without posterior wall puncture. Through study completion,an average of 5 minutes
Primary success in first attempt success puncture and catheterization in first attempt Through study completion,an average of 5 minutes
Secondary success overall success catheterization with the maximum of 10 minutes Through study completion,an average of 5 minutes
Secondary time needed to catheterization time required for successful puncturing and catheterization with the maximum of 10 minutes Through study completion,an average of 5 minutes
See also
  Status Clinical Trial Phase
Recruiting NCT04806932 - Comparison of the Modified and Conventional Approach of Radial Artery Cannulation Under Short-axis Ultrasound Guidance in ICU Hypotensive Patients. N/A