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Trials / Recruiting

RecruitingNCT07062861

Proximal and Distal Radial Artery Cannulation in Children

Comparison of Proximal and Distal Cannulation of the Radial Artery by Ultrasonography in Pediatric Patients Undergoing Elective Surgery

Status
Recruiting
Phase
Study type
Observational
Enrollment
50 (estimated)
Sponsor
Marmara University · Academic / Other
Sex
All
Age
4 Years – 14 Years
Healthy volunteers
Not accepted

Summary

Intraarterial cannulation is important for continuous blood pressure monitoring and blood gas analysis throughout the surgical procedure and in intensive care patients. Ultrasonography (USG) has gained popularity in vascular cannulations and facilitates intraarterial interventions. Radial artery is one of the most preferred arteries. Our aim in this study is to compare proximal and distal radial artery cannulations by USG in pediatric patients in terms of procedural success, procedure time and complications.

Detailed description

After the patients are admitted to the operating room, routine monitoring (electrocardiography, noninvasive blood pressure and peripheral oxygen saturation) will be performed. After appropriate vascular access is provided to the patients, the induction phase of general anesthesia will begin. Anesthesia induction will be left to the choice of the primary anesthesiologist and no protocol will be followed. In case of \>25% drop in blood pressure, 0.1 mcg/kg noradrenaline will be administered intravenously. After the appropriate position is given to the arm of the patient to be treated, radial artery cannulation will be performed with USG obeying asepsis rules. Patients will be divided into 2 groups. The first group will be the patients who will be cannulated at the level of the distal radius (styloid process). For the second group, proximal radial artery cannulation will be performed proximally from the styloid process by measuring 1 cm in patients under 20 kg, 2 cm between 20-30 kg, 3 cm between 30-40 kg, 4 cm between 40-50 kg, and 5 cm in patients over 50 kg. Demographic and clinical characteristics of the patients will be recorded. Catheterization success rates, procedure duration, number of interventions, vessel diameter, hematoma at the site of intervention on the 1st postoperative day, circulatory disturbance will be examined.

Conditions

Timeline

Start date
2025-08-28
Primary completion
2026-01-01
Completion
2026-01-01
First posted
2025-07-14
Last updated
2025-12-11

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT07062861. Inclusion in this directory is not an endorsement.