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Study identifier: NCT04576078 Synced from ClinicalTrials.gov · July 28, 2026
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Post-operative Analgesic Effect of Oral Nefopam

Condition: Postoperative Pain After a Total Knee Arthroplasty  ·  Sponsor: Hospices Civils de Lyon

PhasePhase 2
Planned participants50
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

Primary knee arthroplasty by total prosthesis is a painful surgery, performed on patients with advanced gonarthrosis (stage III), thus already presenting hyperalgesia and hyperalgesia and allodynia. This terrain makes the risk of postoperative hyperalgesia but also of persistent postoperative risk of persistent post-surgical pain. Nefopam is a non-opioid centrally acting analgesic drug used as a part of multimodal analgesia. The opioid-sparing effect of nefopam is still controversial across various surgical procedures. In France nefopam is only available as a parenteral formulation; however it is often administered orally. There is currently no study addressing the efficacy of oral nefopam for the postoperative pain management including pain prevention. The investigators conduct a prospective, double-blinded randomized controlled study with the main objective to examine the effect of perioperative orally administered nefopam on postoperative pain after a total knee arthroplasty. Secondary objectives include the quantification of wound allodynia, analysis of adverse events, clinical outcomes, and a pharmacokinetic study of orally given nefopam (plasma and cerebrospinal fluid dosage).

This description comes directly from the study's public registry record.

Talk to the study team

Frederic AUBRUN, MD/PHD  ·  4 72 07 26 11  ·  Frederic.aubrun@chu-lyon.fr

Solene PANTEL  ·  4 26 73 27 25  ·  solene.pantel02@chu-lyon.fr

Always discuss trial participation with your own doctor first.

Locations (1)

Département d'Anesthésie Réanimation, Groupement Hospitalier Nord, Hospices Civils de LyonLyon, Lyon, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT04576078