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Study identifier: NCT06775197 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Partial Meniscal Replacement with Spongioflex®

Condition: Partial Meniscal Loss · Lateral Meniscus Partial Loss · Medial Meniscal Partial Loss  ·  Sponsor: Maria-Josef-Hospital Greven

PhasePhase 4
Planned participants40
Who can joinAll sexes, 18 Years to 60 Years
Healthy volunteersNo

About this study

The purpose of this investigator-initiated trial is to evaluate whether the novel graft can prevent/reduce the disadvantages of the previously used replacement materials and shows better results than the group of patients, which were not operated. Since there is currently no alternative made of biological material to this product, this investigator-initiated trial is of great medical and economic importance. The otherwise following arthrosis or knee prosthesis implantation (TKA ) could be prevented or at least postponed. Initial clinical results are promising. An important and sensitive parameter for assessing the postoperative function of the meniscus is the MRI image. Genovese et al. 2007 were able to show in a categorization/classification which magnetic resonance image can be expected in the case of successful incorporation. Several studies have shown that the known clinical knee scores (Lysholm, IKDC, KOOS, VAS pain) improve significantly after successful ingrowth of the meniscus implant.

This description comes directly from the study's public registry record.

Talk to the study team

Clemens Kösters, PD, Dr. med.  ·  +49-2571-502-12001  ·  Clemens.Koesters@mjh-greven.de

Daniel A den Toom, Dr. med  ·  +49-2571-502-12001  ·  daniel.toom@mhj-greven.de

Always discuss trial participation with your own doctor first.

Locations (1)

Maria-Josef-Hospital Greven GmbHGreven, North Rhine-Westphalia, GermanyRecruiting

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Source record: clinicaltrials.gov/study/NCT06775197