Abstract Short Summary
Abstract
Objective:
To evaluate interim outcomes, durability, and patient satisfaction after Rigicon Infla10® IPP implantation in a large single-center Turkish cohort.
Key Findings:
The revision/removal rate was low at 2.4%, with mechanical failure in only 1.2% of patients. No infections occurred. Device survival was 97.6% at 3 years. High satisfaction was reported by 92.4% of patients, demonstrating both clinical safety and acceptance.
Conclusion:
Rigicon Infla10® IPPs showed excellent durability and high patient satisfaction in the largest Turkish series. The findings support its effectiveness and reliability as a first-line surgical option for erectile dysfunction.
Clinical Relevance:
These results provide robust real-world evidence supporting the clinical use of Rigicon Infla10® as a safe and durable IPP, particularly relevant for patients with ED refractory to conservative treatments.
Keywords
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