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.
To qualify for this study, a subject must have at least one intact hip with bone loss attributable to osteoporosis as indicated by a femoral neck DXA T-score of -2.5 or less. Follow-up visits will be conducted at 10 days, 42 days, 12 months, and 24 months after the procedure. Study evaluations at each follow-up visit include general health (physical exam and medical history update), VAS pain (not at 10 days), FES-I (not at 10 days), EQ5D-5L and Parker Mobility. A Timed Up and Go Test is performed at the 10-day, 42-day and 12-month follow-up. Patient satisfaction with outcome of surgery will be asked at the 42-day and the 12-month follow-up. DXA scans and X-rays will be performed at 12 and 24 months.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
150
Subjects with osteoporosis are treated with AGN1 local osteo-enhancement procedure in the proximal femur
AZ Nikolaas
Sint-Niklaas, Antwerpen, Belgium
RECRUITINGFemoral Neck Bone Mineral Density
6% increase in mean femoral neck BMD from preprocedure baseline to 12 months post-procedure of treated hips
Time frame: 12 months
Primary Safety Evaluation
The incidence of all adverse events and serious adverse events occurring post-AGN1 LOEP through the 12 months follow-up period determined to be at least possibly related to the procedure and/or device.
Time frame: 12 months
Total Hip Bone Mineral Density
6% increase in mean total hip BMD from preprocedure baseline to 12 months post-procedure of treated hips.
Time frame: 12 months
Femoral Neck Bone Mineral Density
6% increase in mean femoral neck BMD from preprocedure baseline to 24 months post-procedure of treated hips.
Time frame: 24 months
Total Hip Bone Mineral Density
6% increase in mean total hip BMD from preprocedure baseline to 24 months post-procedure of treated hips.
Time frame: 24 months
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