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Infiltration or Nerve Blocks in Addition to Adductor Canal Block
RECRUITINGN/ASponsored by GCS Ramsay Santé pour l'Enseignement et la Recherche
Actively Recruiting
PhaseN/A
SponsorGCS Ramsay Santé pour l'Enseignement et la Recherche
Started2026-05-04
Est. completion2027-05
Eligibility
Age18 Years+
Healthy vol.Accepted
View on ClinicalTrials.gov →
NCT06920186
Summary
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
Age: 18 Years+Healthy volunteers accepted
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
Conditions3
ArthritisGonarthrosisTotal Knee Arthroplasty
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Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.
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Actively Recruiting
PhaseN/A
SponsorGCS Ramsay Santé pour l'Enseignement et la Recherche
Started2026-05-04
Est. completion2027-05
Eligibility
Age18 Years+
Healthy vol.Accepted
View on ClinicalTrials.gov →
NCT06920186