Clinical Trials Directory

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

TypeNameDescription
DRUG0.25% BupivacainePeriarticular injection with 20 ml of 0.25% bupivacaine before wound closure.
DRUG0.9% normal salinePeriarticular 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.