Trials / Completed
CompletedNCT01364194
Local Infiltration With Bupivacaine to Increase Quality of Post-operative Pain Control in Total Knee Replacement
Periarticular Injection With Bupivacaine For Post-Operative Pain Control In Total Knee Replacement: A Prospective Randomized Double-Blind Controlled Trial
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 60 (actual)
- Sponsor
- Mahidol University · Academic / Other
- Sex
- All
- Age
- 50 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to evaluate the efficacy of periarticular injection with 0.25% bupivacaine for controlling pain after total knee replacement to improve the quality of post-operative care.
Detailed description
Compare post operative pain control after total knee replacement by periarticular injection with 0.25% bupivacaine compare with 0.9% normal saline.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | 0.25% Bupivacaine | Periarticular injection with 20 ml of 0.25% bupivacaine before wound closure. |
| DRUG | 0.9% normal saline | Periarticular injection with 20 ml of 0.9% normal saline before wound closure. |
Timeline
- Start date
- 2010-03-01
- Primary completion
- 2010-09-01
- Completion
- 2010-09-01
- First posted
- 2011-06-02
- Last updated
- 2011-06-02
Locations
1 site across 1 country: Thailand
Source: ClinicalTrials.gov record NCT01364194. Inclusion in this directory is not an endorsement.