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NCT05736549 · ClinicalTrials.gov registry record · Phase 2
Yale Steroid Enhanced Versus Exparel Nerveblock TKA Part 2
A Phase 2 study of Total Knee Replacement and Knee Arthroplasty, sponsored by Yale University.
- Recruiting
- Registry status
- Phase 2
- Development phase
- 66
- Enrollment target
- 2
- Study locations
NCT05736549 is a Phase 2 study of Total Knee Replacement and Knee Arthroplasty that is actively recruiting participants, run by Yale University. The registered enrollment target is 66 participants, below the 208-participant average among 9 other Total Knee Replacement trials with a reported enrollment target (68% lower). The trial reports 2 study locations across 1 state.
The verdict
NCT05736549, a Phase 2 study of Total Knee Replacement and Knee Arthroplasty, is actively recruiting participants, sponsored by Yale University.
- RECRUITING
- Registry status
- Phase 2
- Development phase
- 66 participants
- Enrollment target
- 2
- Study locations
Study Summary
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 superior analgesia efficacy as compared to B-LB. This study will also assess if perineural B-DEX-MPA results in improved quality of postoperative recovery as compared to B-LB.
Conditions Studied
Interventions
- DRUG Bupivacaine-Liposomal Bupivacaine
- DRUG Bupivacaine -Dexamethasone Sodium Phosphate-Methylprednisolone Acetate
Study Locations (2)
Connecticut
- Yale New Haven Hospital Saint Raphael Campus - New Haven
- Yale New Haven Hospital York Street Campus - New Haven
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 66 participants |
| Start Date | 2023-02-07 |
| Est. Completion | 2028-03 |
| Phase | Phase 2 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05736549
The ClinicalTrials.gov registry entry for NCT05736549 describes a study currently listed as recruiting, categorized as Phase 2. The registered enrollment target is 66 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 208-participant average among 9 other Total Knee Replacement trials with a reported enrollment target (68% lower). The listed sponsor is Yale University, which has 1,492 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Total Knee Replacement appearing as the primary indexed condition, and to 2 interventions - of which Bupivacaine-Liposomal Bupivacaine is the first listed.
NCT05736549 reports 2 study locations spanning 1 distinct geographic area - top geographies include Connecticut.
Frequently Asked Questions
What is clinical trial NCT05736549 about?
NCT05736549 is a clinical study titled "Yale Steroid Enhanced Versus Exparel Nerveblock TKA Part 2". 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 patient...
What is the current status of trial NCT05736549?
This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 66 participants. The study started on 2023-02-07. Estimated completion is 2028-03.
What conditions does trial NCT05736549 study?
This clinical trial studies the following conditions: Total Knee Replacement, Knee Arthroplasty.
What interventions are being tested in trial NCT05736549?
The interventions under investigation include: Bupivacaine-Liposomal Bupivacaine (DRUG), Bupivacaine -Dexamethasone Sodium Phosphate-Methylprednisolone Acetate (DRUG).
Who is sponsoring clinical trial NCT05736549?
This trial is sponsored by Yale University, which has 1,492 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05736549 being conducted?
This trial has 2 study locations across Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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