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Effectiveness Study of the BOA(R)-Constricting IV Band

NCT01104103 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 467

Last updated 2012-08-20

Study results available
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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.

Conditions

  • Catheterization, Peripheral

Interventions

DEVICE

BOA(R)-Constricting IV Band

Device applied in accordance with manufacturer's instructions

DEVICE

Standard elastic constricting band

Standard therapy

Sponsors & Collaborators

  • North American Rescue, LLC

    collaborator UNKNOWN

  • The University of Texas Health Science Center, Houston

    lead OTHER

Principal Investigators

  • Richard N Bradley, M.D. · The University of Texas Health Science Center, Houston

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2010-03-31
Primary Completion
2010-05-31
Completion
2010-05-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01104103 on ClinicalTrials.gov