Nerve Compression Clinical Trial
Official title:
Nerve Function in Healthy Human Volunteers With Two Different Tourniquets
Nerve injury is a serious potential complication associated with the clinical use of exsanguinating tourniquets in surgery. Recently, a novel narrow tourniquet has been proposed, with the claim that it may cause less compression of the nerves. We performed an in vivo comparison of a standard wide tourniquet with the new, narrow tourniquet. Our study specifically looked at neurologic markers in the upper extremity.
The HemaClear â„¢ OHK Medical Device HemaClearâ„¢, approved by FDA, consists of a silicon ring
wrapped in a stockinet sleeve and pull straps (Fig.1). It performs three functions - blood
removal (exsanguinations), arterial flow occlusion, and placement of sterile stockinet 30.
The ring is placed on the extremity and then straps are pulled proximally. The silicone ring
rolls up the limb while the stockinet sleeve unfolds onto the limb. During the rolling up
process, the ring exerts pressure and squeezes the blood away from the limb. Application of
the device takes less than a minute.
The technique behind this device is fundamentally different from classic pneumatic
tourniquets, as pressure is exercised by only a single silicon ring so that the profile is
very small.
Zimmer A.T.S.®3000 The A.T.S.®3000 is an automatic broad tourniquet system with a Limb
Occlusion Pressure (LOP) feature. It is the latest innovation in tourniquet technology and
has FDA approval. It was invented by McEwen 4 and the basic function is described in several
clinical trials and publications 28. The main difference to other pneumatic tourniquets is
the LOP and the Recommended tissue pressure (RTP) feature. These parameters are suitable to
optimize the pressure force on the tourniquet for each individual patient. The LOP is
detected before inflating the tourniquet and the RTP is the LOP plus a safety margin to
guarantee a blood free field (Operator & Service Manual Zimmer A.T.S.® 3000 Automatic
tourniquet system REF 60-3000-101-00).
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Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Open Label
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