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NCT01914705 · ClinicalTrials.gov registry record · NA

Landmark vs. Ultrasound Guided SCVC in the ED

A NA study, sponsored by Antonios Likourezos.

Terminated
Registry status
NA
Development phase
11
Enrollment target

NCT01914705: Clinical Trial NA study, sponsored by Antonios Likourezos.

NCT01914705 is a NA study that was terminated before completion, run by Antonios Likourezos. The registered enrollment target is 11 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01914705, a NA study, was terminated before completion, sponsored by Antonios Likourezos.

TERMINATED
Registry status
NA
Development phase
11 participants
Enrollment target

Study Summary

The objective of the study is to investigate whether or not there will be a significant difference between landmark vs. ultrasound guided approach during Subclavian Central Venous Catheter (SCVC) placement in terms of the success rate, the time it takes to perform the procedure and the complication rate. By using ultrasound to identify anatomical structures that are not seen during the landmark approach, the investigators hypothesize that both the procedural time and the complication rate of ultrasound guided approach should be lower than the landmark approach. The investigators hypothesize that the success rate will be higher in the ultrasound group.

Primary Outcome

Measure whether or not the physician was able to successfully place the subclavian central venous catheter (SCVC).

Interventions

  • PROCEDURE Landmark Procedure
  • PROCEDURE Ultrasound Guided Procedure

Trial Details

FieldValue
Enrollment Target 11 participants
Start Date 2012-02
Est. Completion 2014-10
Phase NA
Antonios Likourezos

33 total trials

Why NCT01914705 stopped before completion

NCT01914705 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 11 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

The record links to 0 conditions, and to 2 interventions - of which Landmark Procedure is the first listed.

NCT01914705 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01914705 about?

NCT01914705 is a clinical study titled "Landmark vs. Ultrasound Guided SCVC in the ED". The objective of the study is to investigate whether or not there will be a significant difference between landmark vs. ultrasound guided approach during Subclavian Central Venous Catheter (SCVC) placement in terms of the success rate, the time it takes to perform the procedure and the complication ...

What is the current status of trial NCT01914705?

This trial is currently terminated. It is a NA study. The enrollment target is 11 participants. The study started on 2012-02. Estimated completion is 2014-10.

What interventions are being tested in trial NCT01914705?

The interventions under investigation include: Landmark Procedure (PROCEDURE), Ultrasound Guided Procedure (PROCEDURE).

Who is sponsoring clinical trial NCT01914705?

This trial is sponsored by Antonios Likourezos, which has 33 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01914705's enrollment target sits among peer trials

11 1927th of 2000 higher than 74 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01914705, the US trial registry maintained by the National Library of Medicine. NCT01914705 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.