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NCT01042613 · ClinicalTrials.gov registry record · NA
A Comparison of the Success Rate Of Cannulation Between The Accuvein Apparatus And Standard Technique
A NA study, sponsored by St. Jude Children's Research Hospital.
- Completed
- Registry status
- NA
- Development phase
- 146
- Enrollment target
NCT01042613 is a NA study that has completed, run by St. Jude Children's Research Hospital. The registered enrollment target is 146 participants.
The verdict
NCT01042613, a NA study, has completed, sponsored by St. Jude Children's Research Hospital.
- COMPLETED
- Registry status
- NA
- Development phase
- 146 participants
- Enrollment target
Study Summary
1. This study will compare the first attempt success rate of cannulation in research participants randomized to using a new FDA approved AccuVein AV300 device for intravenous access with research participants randomized to standard cannulation methods. 2. This study will assess if insertion of intravenous cannula is faster when intravenous access is assisted by the AccuVein AV300 device as compared to the standard technique. 3. This study will assess if the number of skin punctures is fewer when intravenous access is assisted by the AccuVein AV300 device as compared to the standard technique.
Interventions
- PROCEDURE Cannulation using Accuvein device
- PROCEDURE Standard Cannulation method
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 146 participants |
| Start Date | 2010-01 |
| Est. Completion | 2011-03 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01042613
The ClinicalTrials.gov registry entry for NCT01042613 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 146 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is St. Jude Children's Research Hospital, which has 410 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Cannulation using Accuvein device is the first listed.
NCT01042613 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01042613 about?
NCT01042613 is a clinical study titled "A Comparison of the Success Rate Of Cannulation Between The Accuvein Apparatus And Standard Technique". 1. This study will compare the first attempt success rate of cannulation in research participants randomized to using a new FDA approved AccuVein AV300 device for intravenous access with research participants randomized to standard cannulation methods. 2. This study will assess if insertion of intra...
What is the current status of trial NCT01042613?
This trial is currently completed. It is a NA study. The enrollment target is 146 participants. The study started on 2010-01. Estimated completion is 2011-03.
What interventions are being tested in trial NCT01042613?
The interventions under investigation include: Cannulation using Accuvein device (PROCEDURE), Standard Cannulation method (PROCEDURE).
Who is sponsoring clinical trial NCT01042613?
This trial is sponsored by St. Jude Children's Research Hospital, which has 410 total clinical trials registered on ClinicalTrials.gov.
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