A Study to Review Infrapatellar Neurectomy in Primary Total Knee Arthroplasty

Overview

About this study

The primary purpose of this study is to evaluate the incidence of chronic knee pain at 1 year following Total Knee Arthroplasty (TKA). Secondary aims include assessing the incidence of resting pain with Visual Analog Scale (VAS), overall satisfaction with the knee operation (are you satisfied?- yes/no), and the Knee Injury and Osteoarthritis Outcome Score (KOOS Jr.).

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

Primary unilateral Total Knee Arthroplasty (TKA) candidate.

Exclusion Criteria:

Patients who did not undergo a TKA at Mayo Clinic Florida (MCF).

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location	Status	Contact
Jacksonville, Fla. Mayo Clinic principal investigator Glenn Shi, M.D.	Open for enrollment	Contact information: Lori Chase B.S., CCRP (904) 953-3464 Chase.Lori@mayo.edu

Mayo Clinic Location

Status

Contact

Jacksonville, Fla.

Mayo Clinic principal investigator

Glenn Shi, M.D.

Open for enrollment

Contact information:

Lori Chase B.S., CCRP

(904) 953-3464

Chase.Lori@mayo.edu

More information

Publications

Publications are currently not available

Clinical Trials