Verifying the correct placement of central venous catheters
Verification of the Correct Insertion of a Supradiaphragmatic Central Venous Catheter by a Single Echocardiographic Plane
This study tests if using ultrasound to check the placement of central venous catheters can help make sure they are in the right spot and improve patient safety.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 100 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Consorci Sanitari de Terrassa Academic / other |
| Locations | 1 site (Terrassa, Barcelona) |
| Trial ID | NCT06109584 on ClinicalTrials.gov |
What this trial studies
This study aims to assess the accuracy of central venous catheter placement by using ultrasound for initial verification followed by radiographic confirmation in the same patient. The approach focuses on ensuring that the catheter is correctly positioned without altering standard clinical practices. By comparing these two verification methods, the study seeks to enhance patient safety and reduce complications associated with catheter misplacement.
Who should consider this trial
Good fit: Ideal candidates are adults over 18 years old who require a supradiaphragmatic central venous catheter and consent to participate.
Not a fit: Patients with devices that may interfere with ultrasound imaging, poor ultrasound windows, or superior vena cava syndrome may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could significantly reduce the incidence of catheter-related complications in patients requiring central venous access.
How similar studies have performed: While the specific methodology may be novel, similar studies have shown that ultrasound guidance can improve catheter placement accuracy.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients over 18 years of age in whom a decision is made to place a supradiaphragmatic central venous catheter. * Patients who agree to participate in the study Exclusion Criteria: * Patients with devices that may interfere with the ultrasound images. * Patients with poor ultrasound window * Patients with superior vena cava syndrome
Where this trial is running
Terrassa, Barcelona
- Consorci Sanitari de Terrassa — Terrassa, Barcelona, Spain (Recruiting)
Study contacts
- Principal investigator: Paula Gil Esteller, MD — Consorci Sanitari de Terrassa
- Study coordinator: Paula Gil Esteller, MD
- Email: gilesteller@gmail.com
- Phone: +34 628467708
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.