Proximal Humerus Site for Anesthesia
Completed · Not applicable
Conditions studied: Intraosseous Vascular Access
In brief
This will be a prospective, non-controlled study using healthy adult volunteers as subjects receiving bilateral proximal humerus intraosseous (IO) vascular access to evaluate the insertion technique and IO infusion flow rates.
Key facts
- Study ID
- NCT01866514
- Run by
- Vidacare Corporation
- People needed
- 5
- Starts
- 2013-05-01
- Expected to finish
- 2013-06-01
- Last updated by the study team
- 2026-04-17
Who can join
Age: 21 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Age 21 years or older
- Have no amputation of the upper extremities
- Able to lay flat on table for up to 2 hours
- Self-reported as healthy, as confirmed by the PI
You may not qualify if…
- Have an active infection in the body
- Imprisoned
- Pregnant
- Cognitively impaired
- Fracture in humerus, or significant trauma to the site
- Excessive tissue and/or absence of adequate anatomical landmarks in humerus
- Infection in target area
- Humeral IO insertion in past 48 hours, prosthetic limb or joint or other significant orthopedic procedure in humerus
- Current use of anti-coagulants
- Current cardiac condition requiring pacemaker or anti-arrhythmic drugs
- Prior adverse reaction to lidocaine
- Volunteers with any of the following characteristics may be excluded from the infusion pathway evaluation involving administration of contrast dye at the discretion of the PI:
- Prior adverse reaction to contrast dye
- Allergy to any food or drug
- History of impaired renal function
- History of impaired hepatic function
- History of cardiac disease
- History of pheochromocytoma
Where it is running
- Bulverde-Spring Branch EMS — Spring Branch, Texas, United States
Full record on ClinicalTrials.gov
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