A Post-Market Clinical Follow-Up (PMCF) Study to collect clinical data on safety and performance of all TEKNIMED Spine range of products: SPINEFIX, HIGH V+, OPACITY+ and F20 bone cements and mixing and injection systems, and all their private labels. TEKNIMED bone cements are legacy products, some marketed for more than 10 years. Their performance and safety have already been demonstrated by Post-Market Surveillance and previous clinical studies. The current Post-Market Clinical Follow-Up study aims to confirm these claims by collecting data in a "real-life" setting. The study is a retrospective and prospective global, single arm, non-controlled, multicentric, prospective observational study. Patients will be followed as per local standard medical care of the sites.
It is admitted that: * Cementoplasty procedures such as vertebroplasty and kyphoplasty are recommended in the treatment of painful vertebral compression fractures, due to their efficiency and safety * These mini-invasive procedures, where bone cement is injected into a partially collapsed vertebral body, are used to reduce pain and to provide mechanical stability * In most patients, a rapid pain relief and an increase in mobility and quality of life are obtained * Serious complications from bone cements leaks and adjacent vertebral fractures can be observed but remain rather rare * The use of spinal cement in pedicle screw augmentation procedures can be relevant to increase the strength of the screw fixation in the bone, particularly in osteoporotic patients. TEKNIMED has developed several bone cements currently used in vertebroplasty and kyphoplasty procedures in the treatment of vertebral weakness. Among those, one cement is also used in pedicle screw augmentation procedures. With the increasing use of these procedures, there is a need of real-life safety and efficacy data on the bone cements. This retro-prospective study is performed to confirm the safety and performance of TEKNIMED spine bone cements in their current clinical use.
Study Type
OBSERVATIONAL
Enrollment
500
Vertebroplasty is a procedure in which a special medical-grade cement mixture is injected into a fractured vertebra to relieve pain
Kyphoplasty is a procedure in which a special medical-grade cement mixture is injected into a fractured vertebra to relieve pain
Pedicular Screw Augmentation is a procedure in which a special medical-grade cement mixture is injected into pedicular screws in order to augment fixation strength
CHU HautePierre
Strasbourg, Bas-Rhin, France
RECRUITINGPôle Rachis Hôpital Privé d'Eure et Loir
Mainvilliers, Eure et Loir, France
RECRUITINGHôpital Toulouse Purpan
Toulouse, Haute Garonne, France
RECRUITINGPôle Sud Santé
Le Mans, Sarthe, France
RECRUITINGCentre Hospitalier Métropole Savoie
Chambéry, Savoie, France
RECRUITINGHospitale Cruz Vermelha Portuguesa
Lisbon, Portugal
RECRUITINGClínica Teknon Instituto de neurociencias
Barcelona, Spain
RECRUITINGHospital Neurotraumatologico
Granada, Spain
RECRUITINGHospital Clínico Universitario Virgen de la Arrixaca
Murcia, Spain
RECRUITINGFundacio Assistencial Mutua de Terrassa - Edifici Estació
Terrassa, Spain
RECRUITING...and 2 more locations
Alleviation of Pain
Pain evaluated by Visual Analogue Scale (VAS): on a scale of 0 to 10, with 0 being no pain and 10 being the most severe pain at the Baseline and at the Follow-up visits
Time frame: 24 months
Restoration of quality of life
Evaluated through short questions : Oswestry Disability Index (ODI score)
Time frame: 24 months
Patient satisfaction
Evaluated through short questions : A. Are you satisfied with your surgery? Yes/No/Without opinion B. Has your health improved? Yes/Stable/No C. Given the results, would you accept this intervention again? Yes/No/Without opinion
Time frame: 24 months
Stabilization of vertebrae
Radiographic imaging
Time frame: 24 months
Adverse events
All adverse events occured during surgery and through study completion
Time frame: 10 years
Antalgic Consumption
Antalgic consumption and the drug type at the Baseline and at the Follow-up visits
Time frame: 24 months
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