A Retrospective Study to Evaluate the ConforMIS iUni, iDuo & iTotal® KRS
| Status: | Recruiting |
|---|---|
| Conditions: | Arthritis, Arthritis, Osteoarthritis (OA) |
| Therapuetic Areas: | Rheumatology |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 11/11/2018 |
| Start Date: | April 1, 2017 |
| End Date: | April 2019 |
| Contact: | Marc Quartulli |
| Email: | Marc.Quartulli@conformis.com |
| Phone: | 781-345-9191 |
A Retrospective Study to Evaluate the ConforMIS iUni, iDuo & iTotal® CR (Cruciate Retaining) Knee Replacement Systems
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.
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.
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.This study is a retrospective, single-center study, with one single remote follow up
contact. Patients will be contacted either by phone or email for a single remote follow-up.
Retrospective data will be collected from medical records including pre-operative, operative
and any follow up visits which have occurred since implantation as available.
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.This study is a retrospective, single-center study, with one single remote follow up
contact. Patients will be contacted either by phone or email for a single remote follow-up.
Retrospective data will be collected from medical records including pre-operative, operative
and any follow up visits which have occurred since implantation as available.
Inclusion Criteria:
- Previously underwent surgical implantation of a ConforMIS iUni, iDuo or iTotal knee
replacement.
- Subject must be greater than 18 years of age.
We found this trial at
1
site
7593 West Boynton Beach Boulevard
Boynton Beach, Florida 33437
Boynton Beach, Florida 33437
Principal Investigator: Gregory Martin, MD
Phone: 561-236-4174
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