Clinical Trials Directory

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UnknownNCT03777735

Human Bone Graft for Fixation of Osteochondral Defects in the Knee Joint

Multicentric Observational Study on the Use of a Human Bone Graft in Osteochondral Defects

Status
Unknown
Phase
Study type
Observational
Enrollment
20 (estimated)
Sponsor
Medical University of Vienna · Academic / Other
Sex
All
Age
8 Years – 99 Years
Healthy volunteers
Not accepted

Summary

This observational study is to document the application of a human bone graft in the surgical repair of bone fragment detachment in the knee joint (osteochondral defect) and its subsequent healing process.

Detailed description

For the treatment of bone fractures metal screws have been used for decades. Removal of material is the major disadvantage of conventional osteosynthesis and requires a second intervention, with all the complications and risks for each patient. In order to avoid this second surgery, it is possible to use human bone screw grafts instead of metal screws. The bone graft helps to create a solid, bony connection. This connection leads to an extension, a bone remodeling, bone installation and optimal reparation process in the affected area. The comparatively rare occurrence of suitable patients contributes to the fact that there has not been enough systematic research to objectively confirm the benefits of the product, which is why this observational study is being conducted. In total, 20 patients will be enrolled in several centers in Austria. The low number of cases and the multicenter design is due to the rarity of suitable patients. This observational study will use Shark Screw® grafts without exception at all participating centers. These grafts are manufactured by two tissue banks, the Austrian Tissue Bank surgebright and the German Institute for Cell and Tissue Replacement (DZIG) and were approved by the competent Austrian authority (AGES) in 2016. All patients participating in this observational study, due to a medical indication, undergo surgical treatment of osteochondral defects using the bone screws mentioned above. Postoperatively, the patients are observed over a period of 24 months. In total, there are five follow-up examinations during which clinical examinations, x-rays and a magnetic resonance tomography (MRI) is performed. In addition the KOS-ADL and IKDC Score are collected.

Conditions

Interventions

TypeNameDescription
PROCEDUREhuman bone graft screwAll patients undergo surgical treatment of osteochondral defects in the knee joint with human bone graft screws.

Timeline

Start date
2018-04-24
Primary completion
2023-04-01
Completion
2024-04-01
First posted
2018-12-17
Last updated
2022-08-24

Locations

5 sites across 1 country: Austria

Source: ClinicalTrials.gov record NCT03777735. Inclusion in this directory is not an endorsement.