Optimizing Local Anesthetic Concentration for Continuous Femoral Nerve Blocks



Status:Archived
Conditions:Orthopedic
Therapuetic Areas:Orthopedics / Podiatry
Healthy:No
Age Range:Any
Updated:7/1/2011
Start Date:June 2009
End Date:December 2010

Use our guide to learn which trials are right for you!


This is a randomized, observer-masked, controlled study. Subjects will be patients
undergoing bilateral total knee arthroplasty (TKA). One side (left or right) will be
randomized to one of two treatment groups: a postoperative ropivacaine concentration of 0.1%
or 0.4%. The contralateral side will receive the other possible ropivacaine concentration of
0.1% or 0.4%. The basal rate and patient-controlled bolus volume will depend upon the
treatment group, but the total dose of local anesthetic is the same for each. For the
duration of the study, all patients will receive the current usual and customary analgesics
for bilateral TKA patients. All patients will receive a ropivacaine perineural infusions
initiated in the operating room and continued until at least the afternoon of postoperative
day (POD) 2, as well as oral acetaminophen, a sustained-release oral opioid; and celecoxib.
Rescue opioid and route of administration will be determined by pain severity using a
Numeric Rating Scale of 0-10, with 0 equal to no pain and 10 being the worst imaginable
pain.


The investigators propose to test the null hypothesis that differing concentrations of
ropivacaine (0.1% vs. 0.4%) at an equal total dose has no impact on quadriceps muscle
strength during a continuous femoral nerve block following total knee arthroplasty (TKA).
These results will help define the optimal concentration of local anesthetic used for
continuous peripheral nerve blocks.


We found this trial at
1
site
Cleveland, Ohio 44195
?
mi
from
Cleveland, OH
Click here to add this to my saved trials