Adaptive Pudendal Nerve Stimulation: A Pilot Study on Safety, Technical Feasibility, and Clinical Effect
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This pilot study aimed to evaluate the safety, technical feasibility, and clinical outcomes of a new adaptive pudendal nerve stimulation device in women with treatment-refractory urinary incontinence. The results indicated that the device was safe and technically feasible, with significant reductions in incontinence episodes and improvements in quality of life reported by patients at the six-month follow-up. Additionally, the adaptive stimulation feature was utilized by 70% of participants, further enhancing therapeutic outcomes.
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