Yale Steroid Enhanced Versus Exparel Nerveblock TKA RCT Study

Recruiting Phase 2 Interventional Study
Total Knee Replacement Knee Arthroplasty
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Supportive Care
Participants needed
250 (estimated)
Sponsor
Yale University · Other
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About This Trial
The objective of this phase 2 study is to investigate the efficacy of Dexamethasone sodium phosphate (DEX) plus Methylprednisolone acetate (MPA) in combination with plain bupivacaine (B) compared with Liposomal Bupivacaine (LB) in combination with plain bupivacaine on post-surgical pain control among patients undergoing unilateral total knee arthroplasty (TKA) to asses if perineural B-DEX-MPA will…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * American Society of Anesthesiologists status I, II and III, elective, primary, unilateral TKA planned for spinal anesthesia with plain 0.5% bupivacaine. Exclusion Criteria: * Refusal of consent * Pregnancy * Conditions making the patient unable to fill out questionnaire onli…
Contacts

Jinlei Li, MD PhD

475-434-4038

jinlei.li@yale.edu

CONTACT