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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: Completed NA study, sponsored by St. Jude Children's Research Hospital.
NCT01042613 is a NA study that has completed, run by St. Jude Children's Research Hospital. The registered enrollment target is 146 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (90% lower). According to ClinicalTrials.gov, the official US trial registry.
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.
Primary Outcome
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. There is one timepoint for outcome data collection and it is prior to cannulation. Success (yes) is defined as needle insertion into target vein.
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 |
What the finished NCT01042613 record still lists
NCT01042613 is an interventional study that assigns participants to a tested intervention. The registered 146 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (90% lower).
The record links to 0 conditions, and to 2 interventions - of which Cannulation using Accuvein device is the first listed.
NCT01042613 does not publish any study locations in the registry export this page uses.
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.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01042613's enrollment target sits among peer trials
146 704th of 2000 higher than 1,296 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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