Evaluation of the Latella™ Knee Implant System for Medial Osteoarthritis Pain Reduction
Stopped early · Not applicable
Conditions studied: Osteoarthritis
In brief
The objective of the Latella-US study is to demonstrate the safety and efficacy of the Latella Knee Implant System for the reduction of medial osteoarthritis pain.
Key facts
- Study ID
- NCT02608957
- Run by
- Cotera, Inc.
- People needed
- 1
- Starts
- 2015-12-01
- Expected to finish
- 2017-03-01
- Last updated by the study team
- 2017-04-04
Who can join
Age: 30 and older, up to 70. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- History of pain due to medial osteoarthritis
- Qualifying baseline pain scores
- Kellgren-Lawrence Grades 2-3
You may not qualify if…
- Osteoporosis
- Rheumatoid arthritis
- Joint instability
- Metal ion allergy
- Permanent implant in or around the knee joint
- Prior anterior cruciate ligament reconstruction
Where it is running
- The George Washington University — Washington D.C., District of Columbia, United States
- Rush University Medical Center — Chicago, Illinois, United States
Full record on ClinicalTrials.gov
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