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Study identifier: NCT05574868 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Rigicon Infla10® Three-Piece Inflatable Penile Prosthesis (ERASE ED)

Condition: Erectile Dysfunction  ·  Sponsor: Rigicon, Inc.

PhaseNA
Planned participants182
Who can joinMale, 22 Years to no upper limit
Healthy volunteersNo

About this study

This study evaluates the long-term safety and efficacy of the use of the Rigicon Infla 10® Three-Piece Inflatable Penile Prosthesis in patients with erectile dysfunction. This study follows patients implanted with the Rigicon Infla 10® Three-Piece Inflatable Penile Prosthesis for up to 3 years after implantation. This study will take approximately 6 months to enroll all subjects. (14 days, 6 weeks, 6 months, 12 months,18 months, 24 months, and 36 months, post-procedure. ) Subjects will be followed per protocol and institutional standard of care for ED and comorbidities.

This description comes directly from the study's public registry record.

Talk to the study team

Zeynep Tin Konukcu  ·  888-202-9790  ·  clinical@rigicon.com

Feyzanur CALDIRAN, PhD  ·  888-202-9790  ·  fcaldiran@rigicon.com

Always discuss trial participation with your own doctor first.

Locations (7)

Wesley HospitalAuchenflower, AustraliaRecruiting
Canberra Laparoscopic, Robotic & Laser Urology CentreGarran, AustraliaRecruiting
Katelaris UrologyHornsby, AustraliaRecruiting
St George UrologyHurstville, AustraliaRecruiting
Advanced Urology MelbourneMalvern, AustraliaRecruiting
Shire UrologyMiranda, AustraliaRecruiting
Urology South at Holmesglen Private HospitalMoorabbin, AustraliaRecruiting

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Source record: clinicaltrials.gov/study/NCT05574868