Osteo Arthritis | Continuous Regional Anesthesia for Septic Limb Orthopedic Surgery
Osteo Arthritis research study
What is the primary objective of this study?
This study aims to assess the safety of using continuous regional anesthesia for post-operative analgesia during septic limb orthopedic surgery. The study hypothesis is that continuous regional anesthesia would not induce septic complication in the operated limb and could improve post-operative recovery.
Who is eligible to participate?
Inclusion Criteria: - Osteo arthritis or cellulitis requiring surgical intervention - anatomical possibility of regional anesthesia - age >18 ans - written informed consent Exclusion Criteria: - loco-regional anesthesia impossibility (puncture zone infection, local anesthesics allergie, amiodarone or mexilétine treatment, neurologic deficit for exemple) - patient under tutelle or curatelle - pregnant or beast feeding woman
Which medical condition, disease, disorder, syndrome, illness, or injury is researched?
Interventions can include giving participants drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available or noninvasive approaches such as surveys, education, and interviews.
Drug:Systemic analgesia + Continuous regional anesthesiaSystemic analgesia + Continuous regional anesthesia, peri neural for the 2 to 4 first days post-operative
Drug:Systemic analgesiaSystemic analgesia as usual
Research studies and clinical trials typically have two or more research arms. An arm is a group of people who receive the same treatment in the study.
Continuous regional anesthesia
Start Date: October 2013
Completed Date: November 2015
Primary Outcome: Septic complication in the operated limb
Study sponsors, principal investigator, and references
Lead Sponsor: University Hospital, Strasbourg, France