Trials / Completed
CompletedNCT05765682
Mepivacaine Vs. Bupivacaine Spinal for TKA
Mepivacaine Vs. Bupivacaine Spinal: Effect on Return of Motor Function, Time to Ambulation, and Length of Stay in Total Knee Arthroplasty
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 160 (actual)
- Sponsor
- Medical University of South Carolina · Academic / Other
- Sex
- All
- Age
- 18 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
This study will enroll patients 18-75 years of age who are undergoing elective primary total knee replacement. The patients will be randomized to receive one of two spinal blocks: 1) mepivacaine or 2) bupivacaine. The primary goal is to determine which group arrives at recovery of motor function first. Ultimately, this study will explore if mepivacaine leads to earlier return of motor function and ultimately earlier movement and discharge times following total knee replacement.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Mepivacaine Spinal | spinal block using 60mg of mepivacaine |
| OTHER | Bupivacaine Spinal | spinal block using 10mg of bupivacaine |
Timeline
- Start date
- 2023-03-13
- Primary completion
- 2024-08-23
- Completion
- 2024-08-25
- First posted
- 2023-03-13
- Last updated
- 2024-09-19
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT05765682. Inclusion in this directory is not an endorsement.