NCT07773506

Brief Summary

This prospective observational study aims to evaluate the diagnostic utility of vascular ultrasound for internal jugular vein (IJV) assessment in adult patients undergoing clinically indicated IJV cannulation. Traditionally, bedside clinical assessment of jugular venous pressure (JVP) is challenging and frequently imprecise in critically ill or obese individuals. This study investigates whether non-invasive ultrasound parameters, specifically IJV diameter, collapsibility index, and Doppler flow patterns, can reliably estimate central venous pressure (CVP) and identify elevated JVP. Participants admitted to the Intensive Care Unit, Emergency Department, or Operating Theatres who require right IJV catheterization will receive a standardized pre-procedural vascular ultrasound evaluation in a supine position (0-30° head elevation) prior to routine, ultrasound-guided cannulation. Ultrasound measurements will then be compared to direct central venous pressure readings to assess diagnostic accuracy and correlation.

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
12mo left

Started Sep 2026

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress8%
Sep 2026Oct 2027

First Submitted

Initial submission to the registry

August 15, 2026

Completed
4 days until next milestone

First Posted

Study publicly available on registry

August 19, 2026

Completed
13 days until next milestone

Study Start

First participant enrolled

September 1, 2026

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2027

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2027

Last Updated

August 19, 2026

Status Verified

August 1, 2026

Enrollment Period

1 year

First QC Date

August 15, 2026

Last Update Submit

August 15, 2026

Conditions

Keywords

Internal Jugular VeinVascular UltrasoundUltrasound GuidanceCentral Venous CatheterizationJugular Venous PressureCentral Venous PressureCollapsibility IndexDoppler Flow

Outcome Measures

Primary Outcomes (1)

  • Internal Jugular Vein Collapsibility Index Percentage

    The Internal Jugular Vein (IJV) collapsibility index is evaluated by bedside vascular ultrasound and calculated using the formula: \[(maximum anterior-posterior diameter during expiration - minimum anterior-posterior diameter during inspiration) / maximum anterior-posterior diameter during expiration\] \* 100. The outcome is reported as a continuous percentage from 0% to 100%, where higher values indicate greater vein collapsibility

    Baseline

Study Arms (1)

Ultrasound-Guided IJV Cannulation Cohort

Adult patients in the Intensive Care Unit, Emergency Department, or Operating Theatres requiring ultrasound-guided right internal jugular vein (IJV) cannulation for clinical indications. Participants undergo pre-procedural vascular ultrasound to assess IJV diameter, collapsibility index, and Doppler flow characteristics in the supine position (0-30° head elevation), followed by ultrasound-guided catheterization and comparison with central venous pressure measurements.

Eligibility Criteria

Age18 Years+
Sexall
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Adult patients aged 18 years or older admitted to the Intensive Care Unit (ICU), Emergency Department, or Operating Theatres at Assiut University Hospitals who require ultrasound-guided right internal jugular vein (IJV) cannulation and hemodynamic assessment for clinical indications.

You may qualify if:

  • Adult patients aged 18 years or older.
  • Patients admitted to the Intensive Care Unit (ICU), Emergency Department, or Operating Theatres who require internal jugular vein (IJV) cannulation for clinical indications.
  • Patients in whom ultrasound-guided right internal jugular vein cannulation is planned.
  • Patients who are hemodynamically stable enough to undergo ultrasound examination before cannulation.
  • Patients able to undergo vascular ultrasound examination in the supine position (0-30° head elevation according to the study protocol).
  • Patients in whom complete ultrasound assessment of the internal jugular vein can be performed (including maximum diameter, minimum diameter, cross-sectional area, and collapsibility/distensibility index).
  • Patients with a clinically indicated assessment of central venous pressure (CVP) or jugular venous pressure (JVP) allowing comparison with ultrasound measurements.
  • Patients providing written informed consent, or consent obtained from a legally authorized representative when applicable.

You may not qualify if:

  • Patients younger than 18 years of age.
  • Previous surgery, radiotherapy, or significant trauma involving the neck.
  • Known thrombosis, stenosis, or congenital anomalies of the internal jugular vein.
  • Local infection, cellulitis, burn, or hematoma at the intended cannulation site.
  • Large neck masses, thyroid enlargement, or cervical pathology causing distortion of neck anatomy.
  • Severe coagulopathy or uncontrolled bleeding disorders contraindicating internal jugular vein cannulation.
  • Patients with cervical spine instability or those in whom proper positioning for ultrasound examination is not possible.
  • Inadequate ultrasound visualization of the internal jugular vein.
  • Severe tricuspid valve disease or conditions causing marked alterations in central venous hemodynamics that interfere with accurate interpretation of IJV measurements.
  • Refusal of the patient or legally authorized representative to provide informed consent.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Resident of Diagnostic and Interventional Radiology

Study Record Dates

First Submitted

August 15, 2026

First Posted

August 19, 2026

Study Start

September 1, 2026

Primary Completion (Estimated)

September 1, 2027

Study Completion (Estimated)

October 1, 2027

Last Updated

August 19, 2026

Record last verified: 2026-08