Central venous catheter placement with bedside ECG guidance and thoracic ultrasound
Official title: A Randomised Feasibility Study of Real-time Intracavity ECG and Thoracic Ultrasound for Central Venous Catheter Tip Confirmation in Critical Care
Run by York Teaching Hospitals NHS Foundation Trust · NCT07291869 · Data updated 2026-11-12
This study tests whether using intracavity ECG to confirm catheter tip position and bedside ultrasound to check for pneumothorax is feasible compared with standard post-procedure X-rays.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 75 (estimated) |
| Sponsor | York Teaching Hospitals NHS Foundation Trust Academic / other |
| Drugs / interventions | radiation |
| Locations | 1 site (York, North Yorkshire) |
| Status | Recruiting |
| Started | May 15, 2026 |
| Main results expected | October 2027 |
| Study ends | October 2027 |
| Registry record updated | June 2, 2026 |
| Trial ID | NCT07291869 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults (>=18) requiring internal jugular CVC insertion in a critical care setting who can undergo both IC-ECG and thoracic POCUS.
✕Probably not a fit
Patients with conditions that preclude reliable intracavity ECG interpretation or thoracic ultrasound, or those with exclusion criteria.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This single-center randomized feasibility trial compares standard ultrasound-guided CVC insertion with the addition of intracavity ECG tip confirmation and thoracic POCUS for pneumothorax detection. Eligible adults requiring internal jugular CVC placement are randomized to either the standard approach (ultrasound guidance plus post-procedure X-ray) or the intervention (ultrasound guidance plus IC-ECG tip confirmation and thoracic POCUS). All participants receive a post-procedure chest X-ray for comparison. The study aims to determine if bedside IC-ECG and POCUS can streamline verification and reduce imaging needs without compromising safety. Outcomes focus on feasibility, accuracy of tip location, detection of pneumothorax, and workflow implications.
Why it matters
Potential benefit: If feasible and safe, this approach could shorten verification time and reduce reliance on post-procedure X-ray.
How similar studies have gone: Previous work suggests bedside imaging can aid CVC verification, but this exact combined approach requires prospective feasibility data.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adult (aged ≥ 18 years) * Admitted, or planned for admission, to critical care * Requiring central venous catheter insertion as a part of their usual care * Suitable for both right or left internal jugular vein insertion Exclusion Criteria: * Previously randomised into CVC-TIP * Atrial fibrillation on 12-lead ECG * Cardiovascular instability, defined as * Noradrenaline dose \> 0.5mcg/kg/min * Rapidly escalating doses of vasopressors / inotropes * Difficulty in obtaining thoracic ultrasound images due to either * Weight \> 120kg * Existing pneumothorax (either side) * Subcutaneous emphysema * Wounds / dressing over anterior chest wall * Existing pacemaker * Non-English speaking participants * Death perceived as imminent * Any other reason as determined by treating clinician
Where it's running
-
York and Scarborough Teaching Hospitals NHS Foundation Trust
York, North Yorkshire, United Kingdom Recruiting
Study contacts
- Principal investigator: Andrew Chamberlain, MBChB — York Teaching Hospitals NHS Foundation Trust
- Study coordinator: Andrew Chamberlain, MBChB
- Email: andrew.chamberlain8@nhs.net
- Phone: +441904 631313
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Automated ABPI for Peripheral Artery Disease: A Pilot Look at Two Devices
This pilot checks if two automated ankle-brachial pressure index devices can reliably detect PAD across symptom levels and after bypass surgery, using patient and clinician feedback for practicality.
-
AI-powered personalized exercise plan for older adults using a wearable app
A wearable-enabled, AI-driven exercise app is tested to see if it’s feasible and acceptable for adults 65+ and whether it can help increase activity, improve mood, and boost quality of life.
-
Frailty and Ultrasound-Guided Catheterization in Adult Cardiac Surgery Patients
This study tests whether frailty and ultrasound measurements taken before surgery can predict how difficult it will be to place an ultrasound-guided internal jugular venous catheter in adults undergoing elective cardiac surgery.
-
Which CVC dressing securement helps prevent MARSI best
This study tests three dressing strategies (acrylic tape, silicone tape, and barrier film with acrylic tape) to see which best prevents MARSI in adults with central venous catheters.
-
Behavioral program to help depressed nursing home residents see if it helps
This study tests the InSTILL program to see if it is feasible, satisfactory, and helpful for residents of skilled nursing facilities who have depressive symptoms.
-
LVOT VTI measurements by minimally trained operators in healthy volunteers
This study tests whether medical students or new physicians can measure LVOT VTI with transthoracic echocardiography as accurately as an experienced clinician.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.