Infiltration or Nerve Blocks in Addition to Adductor Canal Block
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorGCS Ramsay Santé pour l'Enseignement et la Recherche
About this trial
The aim of this study is to evaluate the analgesic efficacy of this quadruple sensory block compared with the currently recommended procedure (adductor canal block + infiltration).
Eligibility criteria
Qualifiers
Adult male or female
Patient with signed consent to participate in the study,
Patient with uni or bilateral primary gonarthrosis
Indication for total knee arthroplasty.
Disqualifiers
History of knee fracture, arthroplasty or osteotomy
Known or unknown contraindication to ALR or locoregional anesthesia products
Neurological disease, stroke sequelae
Mental deficiency or any other reason that may hinder understanding or strict application of the protocol
Trial design
Treatments tested in this trial
- Analgesia
- Analgesia
Treatment groups
100 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov