RECONFIRM - Study of AGN1 LOEP in Patients with Osteoporosis
Prospective, Post-market Evaluation of Safety and Efficacy of a Local Osteo- Enhancement Procedure (LOEP) in the Proximal Femur of Women in Europe with Osteoporosis
About This Trial
The research will be conducted as a prospective, post-market, multi-center study within Europe. The maximum number of subjects to be treated is 150 across up to 20 sites. This will be a non-randomized and open-label study. The study will collect procedural, short- and long-term data on the safety and clinical performance of AGN1 LOEP in the post-market setting in European countries where AGN1 LOEP is commercially available. AGN1 is intended to form new bone in voids in the proximal femur of women with osteoporosis.
Who May Be Eligible (Plain English)
Original Eligibility Criteria
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Treatments Being Tested
AGN1 LOEP
Subjects with osteoporosis are treated with AGN1 local osteo-enhancement procedure in the proximal femur