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Multi-Day Evaluation of the TIVA Device

NCT02747147 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 160

Last updated 2017-05-09

No results posted yet for this study

Summary

Prospective, randomized, single-center study to evaluate the ability of the device to collect good quality blood samples from patients with peripheral IV access over the length of their stay.

Conditions

  • Blood Collections Via Peripheral IV Catheter

Interventions

DEVICE

TIVA blood collection device

the device is attached to a peripheral IV catheter for use as a direct blood draw device into a vacuum tube or a syringe

Sponsors & Collaborators

  • Velano Vascular, Inc.

    lead INDUSTRY

Principal Investigators

  • Deborah F Mulloy, PhD, RN · Brigham and Women's Hospital

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-04-12
Primary Completion
2016-11-21
Completion
2016-12-07

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 NCT02747147 on ClinicalTrials.gov