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Completed Not applicable Interventional Accepts healthy volunteers Results available

A Randomized, Study to Evaluate the Iovera° Device in Treating Pain Associated With Total Knee Arthroplasty

ClinicalTrials.gov ID: NCT02284113

Public ClinicalTrials.gov record NCT02284113. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 19, 2026, 1:30 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Post-Market, Multi-Center, Prospective, Double-Blind, Randomized, Controlled Study to Evaluate the Iovera° Device in Treating Pain Associated With Total Knee Arthroplasty

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study will evaluate the iovera° device in treating pain associated with total knee arthroplasty (TKA). This study will also assess if overall pain medication is reduced following TKA and will investigate the relationship between patients treated with the iovera° device and length of hospital stay, pain, patient satisfaction and improved rehabilitation.

Study identification

NCT ID
NCT02284113
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Pacira Pharmaceuticals, Inc
Industry
Enrollment
150 participants

Conditions and interventions

Interventions

Device

Eligibility (public fields only)

Age range
22 Years to 79 Years
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 2014 (Type not available)
Primary completion
May 2016 (Actual)
Completion
Jun 2016 (Actual)
Last update posted
Jan 24, 2024

2014 – 2016

United States locations

U.S. sites
8
U.S. states
6
U.S. cities
8
Facility City State ZIP Site status
University of California San Diego San Diego California 92130 —
Colorado Orthopedic Consultants, P.C. Englewood Colorado 80110 —
Holy Cross Hospital Orthopedic Research Institute Fort Lauderdale Florida 33334 —
Phoenix Clinical Research, LLC Tamarac Florida 33321 —
Cleveland Clinic Florida Weston Florida 33331 —
LSUHSC - Department of Orthopaedics New Orleans Louisiana 70112 —
Cleveland Clinic Cleveland Ohio 44195 —
Rothman Institute Philadelphia Pennsylvania 19107 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02284113, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 24, 2024 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02284113 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →