Ultrasound-Guided BCV and IJV in ICU Patients

NCT07062068 | Not Yet Recruiting

• 1 other identifier: SU-BCV-IJV-2025
• Study Type: interventional
• Target: 100
• Locations: 0 countries
• Sites: N/A

Brief Summary

This is a prospective randomized clinical trial aiming to compare the success rate, complications, and insertion time between ultrasound-guided brachiocephalic vein (BCV) and internal jugular vein (IJV) cannulation in mechanically ventilated patients in the intensive care unit (ICU). The goal is to determine whether BCV access offers a safer or more effective alternative in critically ill patients requiring central venous catheter placement.

Conditions

Ultrasound-Guided Vascular Access; ICU Patients

Keywords

Comparative Study Between Ultrasound-Guided Brachiocephalic Vein and Internal Jugular Vein Cannulation in Mechanically Ventilated ICU Patients

Outcome Measures

Primary Outcomes (1)

• cannulation failure rate

  Failure to cannulate selected vein at 1st attempt

  Baseline

Study Arms (2)

candidates for BCV cannulation

ACTIVE COMPARATOR

Procedure: ultrasound guided Brachiocephalic vein and internal jugular vein cannulation in mechanically ventilated ICU patients

candidates for IJV cannulation

ACTIVE COMPARATOR

Procedure: ultrasound guided Brachiocephalic vein and internal jugular vein cannulation in mechanically ventilated ICU patients

Interventions

ultrasound guided Brachiocephalic vein and internal jugular vein cannulation in mechanically ventilated ICU patients PROCEDURE

For Arm ( candidates for BCV cannulation ) : by ultrasound guided we insert Central venous catheter in BCV under complete aseptic condition For Arm ( candidates for IJV cannulation ) by ultrasound guided we insert central venous catheter in IJV under complete aseptic conidtion we do comparison between the 2 arms as regard : 1st pass success rate , complications and failure rate in ventilated patient in ICU .

candidates for BCV cannulation; candidates for IJV cannulation

Eligibility Criteria

• Age: 18 Years - 50 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64)

You may qualify if:

• patients with age between ( 18 - 50 years old ) ventilated in ICU with need central venous access , with physical status II or III according to ASA classification .

You may not qualify if:

• refusal of relatives of patients
• Any contraindication of Central venous line insertion as thrombocytopenia , coagulopathy …. Etc
• any suspected or documented thrombus inside vein
• any congenital or acquired musculo-skeletal deformities of neck or clavicle
• any active infections or signs of inflammation over insertion site
• any previous procedures performed at the cannulation site

Sponsors & Collaborators

• Sohag University: lead

Central Study Contacts

Hasnaa mohey ibrahim, resident doctor

CONTACT

0201156950052; hasnaa.mohy@med.sohag.edu.eg

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: OTHER
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Resident doctor at department of anesthesia and ICU

Study Record Dates

• First Submitted: July 2, 2025
• First Posted: July 14, 2025
• Study Start: July 1, 2025
• Primary Completion: November 1, 2025
• Study Completion: December 1, 2025
• Last Updated: July 14, 2025

Record last verified: 2025-07