Pain Clinical Trial
Official title:
Real-World Outcomes Study on Subjects Treated With Radiofrequency Ablation
ROSTRA is an international, prospective, non-randomized, single-arm, multi-center, and post-market study to collect real-world safety and effectiveness data on Abbott's IonicRF™Generator and compatible RFA accessories. This post-market study is intended to satisfy EU MDR requirements. The study will enroll up to 180 subjects at up to 10 sites in Europe and the United States. The total duration of the study is expected to be 19 months, including enrollment, data collection from all subjects, and study closeout.
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Status | Clinical Trial | Phase | |
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Active, not recruiting |
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