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A Retrospective Study to Evaluate the ConforMIS iUni, iDuo & iTotal® KRS

NCT03152357 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 950

Last updated 2023-10-25

No results posted yet for this study

Summary

This study is designed to evaluate implant survivorship, patient satisfaction, and patient-reported outcomes of subjects who have undergone surgery with any of the following ConforMIS knee implants: the iUni®, iDuo® or iTotal® Cruciate Retaining (CR) Knee Replacement Systems.

Conditions

Interventions

DEVICE

ConforMIS iUni, iDuo, or iTotal (CR)

ConforMIS iUni, iDuo, or iTotal (CR)

Sponsors & Collaborators

  • Restor3D

    lead INDUSTRY

Principal Investigators

  • Gregory Martin, MD · JFK Medical Center

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-04-01
Primary Completion
2019-09-01
Completion
2019-12-31
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03152357 on ClinicalTrials.gov