Infiltration or Nerve Blocks in Addition to Adductor Canal Block
Recruiting · NCT06920186 · Interventional (participants receive a specific treatment) · Lead sponsor: GCS Ramsay Santé pour l'Enseignement et la Recherche
View the official record on ClinicalTrials.gov →Interventions studied
Analgesia
What this trial is about
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).
Who can take part
Age range
18 Years and older
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)
Inclusion criteria
- 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.
Exclusion criteria
- 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
- Patient not affiliated to the French social security system
- Patient under court protection, guardianship or curatorship
- Pregnant or potentially pregnant women (women of childbearing age without effective contraception)
- Patient already included in another therapeutic study protocol
Where it is running
2 locations listed.
- Hôpital Privé Claude Galien - Quincy-sous-Sénart, France
- Clinique des Côtes du Rhône - Roussillon, France