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Vein Entry Indicator Device
SU-VEID™ for Intravenous Access in Children
N/A
Waitlist Available
Led By Michael Nemergut, MD, PhD
Research Sponsored by Mayo Clinic
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be younger than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline
Awards & highlights
Study Summary
This trial will compare the success rates of two different methods for starting an IV in children.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
IV Start first-attempt success rate
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: SU-VEID assisted IV InsertionExperimental Treatment1 Intervention
Pediatric patients in surgical pre-op requiring an IV catheter for surgery will have IV insertion using SU-VEID device
Group II: Standard IV InsertionActive Control1 Intervention
Pediatric patients in surgical pre-op requiring an IV catheter for surgery will have standard IV insertion
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Who is running the clinical trial?
Mayo ClinicLead Sponsor
3,205 Previous Clinical Trials
3,766,384 Total Patients Enrolled
1 Trials studying Intravenous Access
20 Patients Enrolled for Intravenous Access
Michael Nemergut, MD, PhDPrincipal InvestigatorMayo Clinic
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:Research Study Groups:
This trial has the following groups:- Group 1: SU-VEID assisted IV Insertion
- Group 2: Standard IV Insertion
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Are there any recruitment opportunities for this experiment?
"According to the information displayed on clinicaltrials.gov, this study is no longer actively recruiting patients. It was first posted in late March of 2022 and edited most recently at the start of April that same year. However, there are other trials open for recruitment currently taking place as well."
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