Evaluation of utility of ultrasound guided iPACK block for knee extension after total knee arthroplasty. - Clinical Trial
Email to Participate
katherine.sweeney@duke.edu
What is the Purpose of this Study?
We are doing this study to learn more about how the study drug (iPACK) can help long-term recovery after a knee replacement.
What is the Condition Being Studied?
Knee Replacement
Who Can Participate in the Study?
- Adults 18-75
- Having a total knee replacement
Age Group
Adults
What is Involved?
If you agree to join this study you will:
- Be randomized (like flipping a coin) to get the study drug (iPACK- a nerve block) or a placebo (harmless medicine)
- Be looked at by a physical therapist after surgery
.
Study Details
Full Title
Evaluation of utility of ultrasound guided iPACK block for knee extension after total knee arthroplasty.
Principal Investigator
Anesthesiologist
Protocol Number
IRB:
PRO00070573
NCT:
NCT03353233
Phase
Phase
IV
ClinicalTrials.gov
View on ClinicalTrials.gov
Enrollment Status
Open for Enrollment
Participate