The primary objective is to demonstrate a longer period of neurologic recovery from a sensory block assessed in each test group versus the group without metabolic disease.
Study Type
OBSERVATIONAL
Enrollment
120
Patients will have a truncal block during hand or wrist surgery.
Centre Hospitalier Universitaire de Nîmes
Nîmes, Gard, France
Hôpital Lapeyronnie CHU de Montpellier
Montpellier, France
Hôpital Privé Claude Galien
Quincy-sous-Sénart, France
The duration of sensory block in minutes.
The duration of the sensory block in minutes. The beginning of this term is defined by the end of the axillary block (last injection), and the end of this period is defined by the reappearance of sensitivity to touch in the area anesthetized.
Time frame: Day 0 (per-op)
Time necessary for completion of axillary blocks (1 / 3 upper humerus)(min)
Time frame: Day 0 (per-op)
Time necessary for installing sensory and motor block (min)
Time necessary for installing sensory and motor block (min): defined by the delay between the end of the block injection and the occurrence of insensitivity of blocked territories
Time frame: Day 0 (per-op)
Failure of the block: yes / no
Failure of the block: yes / no: defined by an absence of sensory block
Time frame: Day 0 (per-op)
Presence of paresthesia: yes / no
Time frame: Day 0 (per-op)
Occurrence of neurological complications, yes/no
Neurological: occurrence of complications (paresthesia, paralysis, paresis ....) that persist (or not) until the final postoperative evaluation
Time frame: Day 0 (post-op)
Occurrence of neurological complications, yes/no
Occurrence of neurological complications (paresthesia, paralysis, paresis ....)
Time frame: 1 month
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