Ultrasound-Guided IV Access for Rescue Peripheral IV Access
Age: Any Age
Sex: Any
Trial Phase: Academic
Sponsor: Mayo Clinic
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
What You Need to Know Before You Apply
What is the purpose of this trial?
The purpose of this study is to assess the anatomy of the great saphenous vein at the level of the medial thigh in the general population in an effort to categorize this as a reliable target vessel for rescue peripheral IV access.
Who Is on the Research Team?
TK
Tobias Kummer, MD
Principal Investigator
Mayo Clinic
Are You a Good Fit for This Trial?
This trial is open to both children and adults who visit or work in the emergency department, as well as those at additional training sites with emergency medicine residents. It's not for critically ill patients, those with inaccessible legs due to dressings or wounds, leg infections/injuries, prisoners, or anyone unable to consent verbally.Inclusion Criteria
I am either a patient or employee in the emergency department or at a training site for emergency medicine.
Exclusion Criteria
Patients that are prison inmates and patients/patient's surrogates who are unable to give verbal consent/assent
My legs are not accessible for examination due to dressings or wounds.
Critically ill patients as determined by the Emergency Medicine consultant of record for the patient
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Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
2-4 weeks
Ultrasound Assessment
Ultrasound of the great saphenous vein at the medial thigh to assess its anatomy
12 months
Follow-up
Participants are monitored for safety and effectiveness after ultrasound assessment
4 weeks
What Are the Treatments Tested in This Trial?
Interventions
- US of the GSV
Trial Overview The study aims to evaluate the great saphenous vein (GSV) at the upper part of the inner thigh using ultrasound (US) technology. The goal is to determine if this vein can be a dependable option for inserting an IV when other veins are not usable.
How Is the Trial Designed?
1Treatment groups
Experimental Treatment
Group I: US of GSVExperimental Treatment1 Intervention
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Who Is Running the Clinical Trial?
Mayo Clinic
Lead Sponsor
Trials
3,427
Recruited
3,221,000+
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