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A Study to Evaluate SU-VEID™ for Improving Peripheral Venous Access Success in Children

NCT05204082 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 169

Last updated 2024-05-23

Study results available
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Summary

The purpose of this study is to determine if use of the SU-VEID™ in children facilitates an increase success rate of peripheral intravenous starts, in comparison to the conventional method of vein entry techniques.

Conditions

  • Intravenous Access

Interventions

DEVICE

Single Use Vein Entry Indicator Device

Electronic pressure sensing device, integrated to a conventional needle catheter, and which indicates continuously during intravenous cannulation whether the tip of the needle is inside or outside of a vein, to assist a clinician in intravenous cannulation.

Sponsors & Collaborators

Principal Investigators

  • Michael Nemergut, MD, PhD · Mayo Clinic

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Max Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-03-28
Primary Completion
2022-07-21
Completion
2022-07-21
FDA Device
Yes

Countries

  • United States

Study Locations

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Entities

Companies

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 NCT05204082 on ClinicalTrials.gov