NCT04548882

Calypso Knee System Clinical Sub-study, OUS Continued Evaluation

Continued Evaluation of the Calypso Knee System for Symptom Relief in Subjects With Medial Knee Osteoarthritis, OUS

• Status: Withdrawn
• Phase: N/A
• Study type: Interventional
• Enrollment: 0 (actual)
• Sponsor: Moximed · Industry
• Sex: All
• Age: 25 Years – 65 Years
• Healthy volunteers: Not accepted

Summary

Calypso Knee System Clinical Study, OUS for subjects with symptomatic osteoarthritis of the medial compartment of the knee. The sub-study will achieve continued evaluation of the safety and clinical effectiveness of the Calypso Knee System.

Detailed description

This sub-study will be a single-arm, prospective, multi-center sub-study for continued evaluation of the safety and clinical effectiveness of Calypso Knee System using an additional measure of post-operative activity improvement.

Conditions

• Osteoarthritis, Knee

Interventions

Type	Name	Description
DEVICE	Calypso Knee System	The Calypso Knee System is an extra-capsular knee implant designed to fill the therapeutic gap between conservative care and more invasive surgical interventions for knee osteoarthritis.

Timeline

• Start date: 2020-09-11
• Primary completion: 2021-10-12
• Completion: 2021-10-12
• First posted: 2020-09-16
• Last updated: 2021-11-08

Regulatory

• FDA-regulated device study