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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 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.
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.
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 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01104103
The ClinicalTrials.gov registry entry for NCT01104103 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 467 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is The University of Texas Health Science Center, Houston, which has 732 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which BOA(R)-Constricting IV Band is the first listed.
NCT01104103 reports 0 study locations.
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.
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