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NCT01680666 · ClinicalTrials.gov registry record · NA
A Prospective Trial of Ultrasound Versus Landmark Guided Central Venous Access in the Pediatric Population
A NA study, sponsored by Stanford University.
- Completed
- Registry status
- NA
- Development phase
- 150
- Enrollment target
NCT01680666: Completed NA study, sponsored by Stanford University.
NCT01680666 is a NA study that has completed, run by Stanford University. The registered enrollment target is 150 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01680666, a NA study, has completed, sponsored by Stanford University.
- COMPLETED
- Registry status
- NA
- Development phase
- 150 participants
- Enrollment target
Study Summary
The investigators hypothesized that, in children undergoing venous cannulation for central line placement by pediatric surgeons, ultrasound-guided cannulation leads to an increase in successful venous cannulation at first attempt compared to landmark guided cannulation.
Interventions
- DEVICE Ultrasound
- PROCEDURE central line placement
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 150 participants |
| Start Date | 2009-05 |
| Est. Completion | 2011-12 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01680666
The ClinicalTrials.gov registry entry for NCT01680666 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 150 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Stanford University, which has 1,744 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Ultrasound is the first listed.
NCT01680666 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01680666 about?
NCT01680666 is a clinical study titled "A Prospective Trial of Ultrasound Versus Landmark Guided Central Venous Access in the Pediatric Population". The investigators hypothesized that, in children undergoing venous cannulation for central line placement by pediatric surgeons, ultrasound-guided cannulation leads to an increase in successful venous cannulation at first attempt compared to landmark guided cannulation.
What is the current status of trial NCT01680666?
This trial is currently completed. It is a NA study. The enrollment target is 150 participants. The study started on 2009-05. Estimated completion is 2011-12.
What interventions are being tested in trial NCT01680666?
The interventions under investigation include: Ultrasound (DEVICE), central line placement (PROCEDURE).
Who is sponsoring clinical trial NCT01680666?
This trial is sponsored by Stanford University, which has 1,744 total clinical trials registered on ClinicalTrials.gov.
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