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RECRUITING
NCT05650866
NA

Safety and Tolerability of a Novel Implantable Device for the Treatment of Erectile Dysfunction

Sponsor: Comphya Australia

View on ClinicalTrials.gov

Summary

The goal of this clinical trial is to assess if a new device is safe to use as a potential treatment for erectile dysfunction following radical prostatectomy. The main questions it aims to answer are: * Is the device safe? * Does the device works well? Are the participants satisfied with the device? Participants will be implanted with the device during the ongoing prostatectomy surgery and will be asked to complete the following tasks during 6 months follow-up: * Come to the hospital for follow-up visits, * Complete questionnaires, * Activate the device every day, * Measure erection hardness. Researchers will compare an implanted group (participants having the device) with a control group (participants not having the device) to see if the device works well.

Official title: Safety and Tolerability of a Novel Implantable Device for the Treatment of Erectile Dysfunction Following Radical Prostatectomy

Key Details

Gender

MALE

Age Range

30 Years - 70 Years

Study Type

INTERVENTIONAL

Enrollment

20

Start Date

2023-05-19

Completion Date

2026-08-31

Last Updated

2026-03-18

Healthy Volunteers

No

Interventions

DEVICE

Activation of pro-erectile nerves within the pelvic plexus

The study device is an active implantable device. The device activates the cavernous nerves by delivering electrical pulses, to trigger an on-demand erection. The daily delivery of electrical pulses to the cavernous nerves will also allow participants to recover natural erectile function.

Locations (4)

St. Vincent's Private Hospital

Fitzroy, Victoria, Australia

Royal Melbourne Hospital

Melbourne, Victoria, Australia

Australian Prostate Centre

North Melbourne, Victoria, Australia

Epworth HealthCare

Richmond, Victoria, Australia