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.
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