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NCT01104103 · ClinicalTrials.gov registry record · NA
Effectiveness Study of the BOA(R)-Constricting IV Band
A NA study, sponsored by The University of Texas Health Science Center, Houston.
- Terminated
- Registry status
- NA
- Development phase
- 467
- Enrollment target
NCT01104103: Clinical Trial NA study, sponsored by The University of Texas Health Science Center, Houston.
NCT01104103 is a NA study that was terminated before completion, run by The University of Texas Health Science Center, Houston. The registered enrollment target is 467 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (67% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01104103, a NA study, was terminated before completion, sponsored by The University of Texas Health Science Center, Houston.
- TERMINATED
- Registry status
- NA
- Development phase
- 467 participants
- Enrollment target
Study Summary
The purpose of this study is to determine whether the BOA(R)-Constricting IV Band is superior to standard methods for starting an IV.
Primary Outcome
This outcome will measure self-reported success at starting the peripheral intravenous lines in the upper extremity of adults. Success is defined as an IV line through which blood may be aspirated and flushes freely without evidence of fluid extravasation. To be successful, the IV must be placed within a maximum of three attempts. We will report the number and percentage of patients with successful for both therapies.
Interventions
- DEVICE BOA(R)-Constricting IV Band
- DEVICE Standard elastic constricting band
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 467 participants |
| Start Date | 2010-03 |
| Est. Completion | 2010-05 |
| Phase | NA |
Why NCT01104103 stopped before completion
NCT01104103 is an interventional study that assigns participants to a tested intervention. The registered 467 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 (67% lower).
The record links to 0 conditions, and to 2 interventions - of which BOA(R)-Constricting IV Band is the first listed.
NCT01104103 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01104103 about?
NCT01104103 is a clinical study titled "Effectiveness Study of the BOA(R)-Constricting IV Band". The purpose of this study is to determine whether the BOA(R)-Constricting IV Band is superior to standard methods for starting an IV.
What is the current status of trial NCT01104103?
This trial is currently terminated. It is a NA study. The enrollment target is 467 participants. The study started on 2010-03. Estimated completion is 2010-05.
What interventions are being tested in trial NCT01104103?
The interventions under investigation include: BOA(R)-Constricting IV Band (DEVICE), Standard elastic constricting band (DEVICE).
Who is sponsoring clinical trial NCT01104103?
This trial is sponsored by The University of Texas Health Science Center, Houston, which has 732 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01104103's enrollment target sits among peer trials
467 222nd of 2000 higher than 1,779 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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