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Clinical Trial Summary

The study is a randomized, prospective, multicenter, controlled clinical trial of the Episealer Knee System. The Episealer Knee System is intended for subjects with up to two focal femoral knee chondral or osteochondral lesion that is causing pain and/or disability and requires surgical treatment.


Clinical Trial Description

The primary objective of this study is to evaluate the safety and clinical effectiveness of the Episealer Knee System (Episealer Trochlea Solo, Episealer Femoral Twin, and Episealer Condyle Solo) compared to microfracture (with or without debridement) in a group of subjects that require repair of up to 2 focal femoral chondral or osteochondral lesions in the knee. Clinical success will be analyzed via subject reported outcomes to measure function and pain improvements as compared to baseline, incidence of secondary surgical interventions for the treated knee, absence of subsidence or migration through radiographic assessment, and assessment of weight-bearing status. ;


Study Design


Related Conditions & MeSH terms

  • Degenerative Lesion of Articular Cartilage of Knee

NCT number NCT04000659
Study type Interventional
Source Episurf Medical Inc.
Contact Katarina Flodström
Phone 1 686 845 9447
Email Katarina.Flodstrom@episurf.com
Status Recruiting
Phase N/A
Start date June 18, 2020
Completion date June 2028

See also
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Active, not recruiting NCT02345564 - Clinical and Radiological Results of Osteochondral Repair Using MaioRegen in Knee and Ankle Surgery N/A
Completed NCT02285725 - Microdrilling Surgery for Full Thickness Chondral Lesions of the Knee Augmented With Concentrated Bone Marrow Aspirate, Platelet Rich Plasma and Hyaluronic Acid N/A
Terminated NCT02981355 - Randomized Evaluation of BST-CarGel Versus Microfracture Alone On Recovery From Distal Femoral Cartilage Lesions Phase 4
Completed NCT01554878 - Observational Study on the Treatment of Knee Osteochondral Lesions of Grade III-IV N/A
Completed NCT01576159 - Serum Cartilage Oligomeric Matrix Protein Levels After 12 Weeks of Different Exercises Phase 0
Active, not recruiting NCT01329445 - DeNovo NT Longitudinal Data Collection (LDC) Knee Study N/A
Completed NCT01605201 - Tissue Engineered Nasal Cartilage for Regeneration of Articular Cartilage Phase 1