Status:
COMPLETED
Proximal Humerus Site for Anesthesia
Lead Sponsor:
Vidacare Corporation
Conditions:
Intraosseous Vascular Access
Eligibility:
All Genders
21+ years
Phase:
NA
Brief Summary
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 a...
Detailed Description
When using IO access in the perioperative and OR settings, abduction of the arms to the shoulder level prevents use of the traditional proximal humerus insertion site due to the rotation of the humera...
Eligibility Criteria
Inclusion
- 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
Exclusion
- 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
Key Trial Info
Start Date :
May 1 2013
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
June 1 2013
Estimated Enrollment :
5 Patients enrolled
Trial Details
Trial ID
NCT01866514
Start Date
May 1 2013
End Date
June 1 2013
Last Update
June 6 2014
Active Locations (1)
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1
Bulverde-Spring Branch EMS
Spring Branch, Texas, United States, 78070