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Disc Disease Degenerative
Clinical trial pipeline · Data from ClinicalTrials.gov
See which Disc Disease Degenerative trials you may qualify forClinical trial pipeline · Data from ClinicalTrials.gov
See which Disc Disease Degenerative trials you may qualify forEfficacy and Safety of Novosis Putty in Transforaminal Lumbar Interbody Fusion for Patients with Lumbar Degenerative Disc Disease : A Pivotal, Randomized, Prosp…
This trial is a real world data (RWD) collection observational study, comprised of both prospective and retrospective arms, that will examine the safety and eff…
A multi-center, prospective, dual arm, randomized, controlled pivotal study to evaluate the safety and effectiveness of the ReGelTec HYDRAFIL™ System.
The goal of this clinical trial is to assess the safety and effectiveness of the study device, CORUS-LX, as an adjunct to lumbar interbody fusion, when used in…
The purpose of this multi-center, prospective, observational registry is to gather information on the clinical outcomes and real-world use of commercially avail…
This is a real world data collection observational study at a single site. There are both prospective and retrospective cohorts. The study will examine the safe…
In accordance with the European Medical Device Regulation MDR 2017/745/EU, the legal manufacturers of medical devices are obliged to evaluate medical devices wi…
This is a real world data collection observational study at a single site. There are both prospective and retrospective cohorts. The study will examine the safe…
The purpose of this post-market clinical study is to evaluate the long-term safety and efficacy of the MEDICREA's systems PASS LP, PASS DEGEN, and PASS Tulip PR…