The aim of this study is to evaluate the performance of the ZENEO needle free device in subcutaneous functioning limits (low performance limit and high performance limit) and for intramuscular injections.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
OTHER
Masking
NONE
Enrollment
97
Sodium Chloride (0.9 %)
Sodium Chloride (0.9 %)
Sodium Chloride (0.9 %)
depth of the injection by MRI
Time frame: 5 minutes after the injection
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