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

Not Applicable

Terminated

• Conditions: Intravenous Access
• Interventions: Device: Single Use Vein Entry Indicator Device

• Registration Number: NCT05204082
• Lead Sponsor: Mayo Clinic

Brief 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.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2022-01-10
• Study First Submitted QC: 2022-01-10
• Study First Posted: 2022-01-24
• Study Start: 2022-03-28
• Primary Completion: 2022-07-21
• Study Completion: 2022-07-21
• Results First Submitted: 2024-04-23
• Status Verified: 2024-05
• Results First Submitted QC: 2024-05-22
• Last Update Submitted: 2024-05-22
• Results First Posted: 2024-05-23
• Last Update Posted: 2024-05-23

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 169

Inclusion Criteria

• Patient age < 18 years old.
• Pediatric patients in surgical pre-op (0-18 years old), requiring an I.V. catheter for surgery who are difficult venous access.
• Written informed consent/ assent from the patient or legal guardian.

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Exclusion Criteria

• Patient age > 18 years old.

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
SU-VEID assisted IV Insertion	Single Use Vein Entry Indicator Device	Pediatric patients in surgical pre-op requiring an IV catheter for surgery will have IV insertion using SU-VEID device

Primary Outcome Measures

Name	Time	Method
Percentage of Participants With IV Access at First Attempt	Baseline	Percentage of participants to have an IV access within the first attempt when using the SU-VEID Device in comparison to the conventional procedure

Trial Locations

Locations (1)

Mayo Clinic Rochester; 🇺🇸 Rochester, Minnesota, United States