Erectile Dysfunction (ED) Clinical Trials

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Evaluation of Penile Prosthesis Pump Manipulation

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Erectile dysfunction is a highly prevalent pathology. When oral or injectable pharmacological treatments prove ineffective, the treatment of choice is penile prosthesis which provides the possibility of sexual activity with penetration. Unfortunately, current prostheses are difficult (or even impossible) to manipulate for some patients. Many patients underutilize their device due to difficulties in using the pump related to mechanical issues (difficult grip, lack of strength, etc.) or sensory issues (altered proprioception, etc.), resulting in an inability to achieve rigidity that allows optimal satisfaction for the patient and/or partners. These difficulties correspond to a significant portion of dissatisfaction among patients with penile prostheses. Actually, no study has evaluated patients' ability to manipulate the pump of their penile prosthesis, as well as the association between these manipulation abilities, the rigidity of erections with a penile prosthesis, and patient and partner sexual satisfaction. In this descriptive study, the primary outcome is to describe the manipulation abilities of patients with penile prostheses during follow-up consultations after prosthesis implantation. The secondary outcomes are to estimate the association of various markers related to penile prosthesis manipulation (overall hand grip strength, pinch grip strength, proprioception, and discrimination) with * Rigidity of erections with penile prosthesis * Patient's sexual satisfaction * Partner's sexual satisfaction * Satisfaction related to pump manipulation

Eligibility
Participation Requirements
Sex: Male
Minimum Age: 18
Healthy Volunteers: f
View:

• The patients will be included based on the following criteria:

• Adults

• Erectile Dysfunction, and had undergone penile prosthesis implantation for more than 3 months

• Able to comprehend the nature and purpose of the research

• Having provided informed consent

⁃ The partner will be included based on the following criteria :

• Adults

• Having a partner who meets the inclusion criteria

• Able to comprehend the nature and purpose of the research

• Having provided informed consent

Locations
Other Locations
France
Department of Urology, Lyon Sud Hospital,
RECRUITING
Pierre-bénite
Contact Information
Primary
Nicolas MOREL-JOURNEL
nicolas.morel-journel@chu-lyon.fr
+ 33 4 72 6788 37
Backup
clément PARAT
clement.parat@chu-lyon.fr
+ 33 4 72 6788 37
Time Frame
Start Date: 2024-06-14
Estimated Completion Date: 2026-12-14
Participants
Target number of participants: 60
Treatments
Other: Patients who have undergone penile prosthesis implantation > 3 months ago and their partner
Evaluation of the manipulation abilities of patients with penile prostheses Evaluation of the rigidity of erections with penile prosthesis, the patient and partner's sexual satisfaction, the satisfaction related to pump manipulation
Related Therapeutic Areas
Sponsors
Leads: Hospices Civils de Lyon

This content was sourced from clinicaltrials.gov