Bone substitutes study after surgery follow-up
Part of Bones, joints & muscles clinical trials.
This study follows patients who receive a Teknimed bone substitute during surgery for bone defects. It collects data on how well these bone fillers work in real-world use.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You are 18 years or older.
- You are not pregnant or breastfeeding.
- You are not under legal guardianship.
- You do not have known allergies to the bone substitute materials used.
- You are scheduled for a surgery that needs a bone filler from this study, or you had such a surgery between 2015 and now.
Quick eligibility check
Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.
Similar studies
Other trials that look related to this one.
This study looks at how a specific bone-repair technique (called induced membrane reconstruction) works in people with large “critical-sized” bone defects. It may help doctors understand the results and properties of this method in both children and adults.
This study is checking how well certain spine cements (used to stabilize broken vertebrae) work in real life. If you are 18 or older and have had or will have a TEKNIMED cement procedure, you may be able to join.
This study is looking at how well Teknimed bone cements and cement restrictors work for people who need a joint replacement (like a hip or knee). If you are scheduled for a joint replacement or have already had one using these products since 2016, you may be able to join.
This study is checking how well people recover after sports surgery using Teknimed products. It is for patients who had or will have a surgery with these products, and aims to see how the products perform in real life.
This study follows patients who receive a new injectable bone filler called Neocement® Inject P during dental reconstructive surgery. The goal is to see if it is safe and works well to help heal bone defects.
This study tracks how well spinal implants (Titania systems) and bone-filling materials (BONEGRAFT) work after surgery and whether patients experience any problems. Researchers will follow patients after cervical or lower spine surgery to confirm these devices are safe and effective in real-world use.
Hear when a new Bone Resorption trial opens
We’ll email you when one opens — at most once a week, no account needed, unsubscribe anytime.