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

Mayo Clinic

Status: Terminated

Conditions: Intravenous Access

Treatments: Device: Single Use Vein Entry Indicator Device

Study type: Interventional

Funder types: Other

Identifiers

NCT05204082

21-006822

Details and patient eligibility

About

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.

Enrollment: 169 patients

Sex: All

Ages: Under 18 years old

Volunteers: Accepts Healthy Volunteers

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.

Exclusion criteria

• Patient age > 18 years old.

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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169 participants in 2 patient groups

Standard IV Insertion

No Intervention group

Description:

Pediatric patients in surgical pre-op requiring an IV catheter for surgery will have standard IV insertion

SU-VEID assisted IV Insertion

Other group

Description:

Pediatric patients in surgical pre-op requiring an IV catheter for surgery will have IV insertion using SU-VEID device

Treatment:

Device: Single Use Vein Entry Indicator Device