Actively Recruiting

Phase 4
Age: 18Years +
All Genders
NCT05534971

Central Line Study

Led by Montefiore Medical Center · Updated on 2026-01-06

160

Participants Needed

1

Research Sites

263 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Two different techniques for placing a central venous catheter will be compared. The studyu team hypothesizes that clinicians randomized to the peripheral catheter technique will have higher first attempt success rates, fewer procedural complications, and a shorter mean time to procedure completion than physicians assigned to wire through hollow bore needle.

CONDITIONS

Official Title

Central Line Study

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patients in the emergency department who require ultrasound guided central line placement
Not Eligible

You will not qualify if you...

  • Inherited, acquired, or medication related coagulopathy or thrombocytopenia (platelets < 100,000)
  • Previous central venous access at the same anatomical site
  • Any indwelling catheter or wire that could potentially interfere with central line placement
  • Anterior border of the target vein deeper than 3.5cm
  • Clinical conditions interfering with informed consent such as dementia, delirium, or encephalopathy as determined by the attending physician

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Montefiore

The Bronx, New York, United States, 10467

Actively Recruiting

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Research Team

J

Joe Offenbacher, MD

CONTACT

B

Benjamin Friedman, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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Central Line Study | DecenTrialz