Posterior Tibial Artery Catheterization

Arterial Catheterization Clinical Trial

Official title:

Real-time Ultrasound-guided Arterial Catheterization in Pediatric Patients: Comparison of Success Rate Among the Arteries

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02912481
• Other study ID #: H-1606-108-771
• Status: Completed
• Phase: N/A
• First received: September 21, 2016
• Last updated: September 4, 2017
• Start date: September 2016
• Est. completion date: July 2017

Study information

• Verified date: September 2017
• Source: Seoul National University Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Arterial catheterization in small children is challenging, even for experienced anesthesiologists. For successful arterial catheterization, the arterial diameter, cross-sectional area, and depth from the skin surface are important considerations, especially in pediatric patients. THe investigators examined the posterior tibial artery (PTA) and dorsalis pedis artery (DPA) using ultrasound (US) to find a reasonable alternative arterial cannulation site to the radial artery (RA) in pediatric patients.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 275
• Est. completion date: July 2017
• Est. primary completion date: March 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: N/A to 2 Years

Eligibility

Inclusion Criteria:

• Patients undergoing general anesthesia needing invasive arterial monitoring

Exclusion Criteria:

• Surgery involving the both hands or foots

Related Conditions & MeSH terms

• Arterial Catheterization

Intervention

Procedure:
• posterior tibial artery

• radial artery

• dorsalis pedis artery

Locations

Country	Name	City	State
Korea, Republic of	SNUH	Seoul	Jongro Gu

Sponsors (1)

Lead Sponsor	Collaborator
Seoul National University Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	first access success rate		immediate after anesthetic induction, maximum 10 minutes