Comparison of the success rate and complications in internal jugular vein cannulation in the first attempt between two ultrasound-guided and 22G needle-guided methods

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20240512061751N1

Enrollment

Registered

2025-03-02

Start date

2024-06-05

Completion date

Unknown

Last updated

2025-07-21

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

Conditions

Presence of other specified functional implants. Presence of other specified functional implants

Interventions

Intervention 1: Intervention group: Ultrasound-guided cannulation. This is done by placing the ultrasound probe slightly above the patients clavicle. When the constricting vein is visible, the main ne

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patient requiring central venous access

Exclusion criteria

Exclusion criteria: Hematoma or abscess at the catheter insertion site prior to the current catheter insertion procedure Patients' personal desire to withdraw from the study

Design outcomes

Primary

Measure	Time frame
Success in cannulation. Timepoint: simultaneous with cannulation. Method of measurement: Ultrasound.	—

Secondary

Measure	Time frame
Complications. Timepoint: simultaneous with cannulation. Method of measurement: Surgeon's evaluation.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAlireza Khazaei

Zahedan University of Medical Sciences

alirezakhazei@gmail.com+98 54 3329 5570

Outcome results

None listed

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