Feasibility of the Latella Implant System for Medial Osteoarthritis (OA)

Evaluation of the Latella Implant System for Lateralization of the Iliotibial Band to Offload the Medial Condyle for Pain Relief in Patients With Medial Osteoarthritis - A Safety Study

Status

Terminated

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT02002637

Enrollment

Registered

2013-12-06

Start date

2013-11-30

Completion date

2017-04-30

Last updated

2017-04-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Osteoarthritis

Brief summary

The objective of this study is to evaluate the safety and technical feasibility of implanting the Latella Implant System in the treatment of patients with medial osteoarthritis of the knee.

Interventions

DEVICELatella Knee Implant System

Study design

Allocation

Intervention model

SINGLE_GROUP

Primary purpose

DEVICE_FEASIBILITY

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

30 Years to 65 Years

Healthy volunteers

Inclusion criteria

* History of pain as due to medial osteoarthritis

Exclusion criteria

* Rheumatoid arthritis * Joint or ligament instability * Metal ion allergy

Design outcomes

Primary

Measure	Time frame
Freedom from unanticipated serious adverse device effects	12 Months

Countries

Netherlands, United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026