Clinical Trial

Early and Late Effects of Nefopam in Multimodal Analgesia After Total Hip Arthroplasty (NEFARTHRO)

Study acronym: NEFARTHRO
Not Yet Recruiting Phase 3
View on ClinicalTrials.gov →
Summary
NEFARTHRO is a multicentric randomized controlled trial comparing the effects of discontinuous infusions of nefopam (bolus) versus continuous infusion of intravenous nefopam (via an infusion pump) versus placebo on the opioid-request during the first 24 hours following a Total Hip arthroplasty, as part of multimodal analgesia including at least paracetamol and a Non-Steroidal Anti-Inflammatory Drug (NSAID). The primary endpoint is cumulative morphine consumption for the first postoperative 24 hours, expressed in mg of iv equivalent morphine, including titration in the Post Anesthesia Care Unit (PACU). Patients will be followed during 6 months.
Trial Details
NCT Number NCT06349798
Lead Sponsor University Hospital, Tours
Conditions Total Hip Arthroplasty
Enrollment 546 participants
Start Date 2024-04
Primary Completion 2026-09 (estimated)
Study Completion 2027-04 (estimated)
Updated on ClinicalTrials.gov 2024-04-05