Yale Steroid Enhanced Versus Exparel Nerveblock TKA Part 2

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
66 (estimated)
Sponsor
Yale University · Other
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About This Trial
The objective of this study is to investigate the efficacy of Dexamethasone sodium phosphate plus Methylprednisolone acetate in combination with plain bupivacaine ((B-DEX-MPA) compared with Liposomal Bupivacaine in combination with plain bupivacaine (B-LB) on post-surgical pain control among patients undergoing bilateral total knee arthroplasty (TKA) to asses if perineural B-DEX-MPA will result in…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * American Society of Anesthesiologists status I, II and III, elective, primary, bilateral 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 onlin…
Contacts

Jinlei Li, MD PhD

475-434-4038

jinlei.li@yale.edu

CONTACT