The aim of this study is to evaluate if memantine administered during 4 weeks beginning 2 weeks before surgery induces a decrease of painful intensity 3 months after surgery, compared to placebo group.
The aim of this study is to evaluate if memantine administered during 4 weeks beginning 2 weeks before surgery induces a decrease of painful intensity 3 months after surgery, compared to placebo group.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
PREVENTION
Masking
NONE
Enrollment
43
The aim of this study is to evaluate if memantine administered during 4 weeks beginning 2 weeks before surgery induces a decrease of painful intensity 3 months after surgery, compared to placebo group.
The aim of this study is to evaluate if memantine administered during 4 weeks beginning 2 weeks before surgery induces a decrease of painful intensity 3 months after surgery, compared to placebo group.
CHU Clermont-Ferrand
Clermont-Ferrand, France
average painful intensity
Time frame: 5 days before visit of 3 months
Evaluation of pain by numerical scale
Time frame: during 15 first days following surgery and to visit of 3 months
Average painful
Time frame: on 5 days before visit of 6 months post-surgery
analgesic consumption
Time frame: during 3 months after surgery
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