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Not yet recruiting NCT07062068

Ultrasound-Guided BCV and IJV in ICU Patients

No phase Interventional Ultrasound-Guided Vascular Access ICU Patients

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: ultrasound guided Brachiocephalic vein and internal jugular vein cannulation in mechanically ventilated ICU patients.
Who it may be relevant to
Registry conditions: Ultrasound-Guided Vascular Access, ICU Patients. Basic parameters: 18 years — 50 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

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

Overview

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.

Detailed description

Central venous cannulation is a common and essential procedure in the management of critically ill patients, especially those requiring mechanical ventilation. Traditionally, the internal jugular vein (IJV) has been the preferred site. However, the brachiocephalic vein (BCV) has recently gained attention due to its potentially favorable anatomical location and reduced complication rates.

This study is designed to compare the outcomes of ultrasound-guided cannulation of the BCV versus the IJV, focusing on parameters such as success rate of insertion on first attempt, total cannulation time, and incidence of complications such as arterial puncture, pneumothorax, or hematoma formation. The study will be conducted on adult patients admitted to the ICU and undergoing mechanical ventilation

Interventions

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

Primary outcome measures

  • cannulation failure rate [Time frame: Baseline]

Eligibility criteria

Inclusion criteria

100 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 .

Exclusion criteria

  • 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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Other

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07062068 · SU-BCV-IJV-2025

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗