Pain Control With Pre-operative Cryoneurolysis Following TKA

Withdrawn before enrolling · Not applicable

Conditions studied: Osteo Arthritis Knee

In brief

The purpose of this study is to assess the potential benefit of preoperative cryoneurolysis in postoperative pain management of total knee arthroplasty patients over current pain management protocol.

Key facts

Study ID

NCT03818022

Run by

Fondren Orthopedic Group L.L.P.

People needed

0

Starts

2019-02-01

Expected to finish

2020-12-01

Last updated by the study team

2024-02-23

Who can join

Age: 18 and older, up to 90. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• any patient scheduled for primary total knee arthroplasty(TKA)

You may not qualify if…

• Bilateral TKA (patients routinely receive spinal anesthesia)
• Minors
• Patients reporting a history of Raynaud's disease
• Patients with an open and/or infected wound on surgical knee
• Patients who are taking opioids during the pre-operative period due to knee pain
• Patients who cannot return for the cryoneurolysis treatment 7 days prior to surgery or post-operative clinical visits
• Patients whose insurance would deny payment for the cryoneurolysis treatment
• Pregnant patients
• Patients unable to speak and read English

Where it is running

• Fondren Orthopedic Group, L.L.P. — Houston, Texas, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.