Purpose of this Study
We are doing this study to learn more about the impact that penile prosthesis devices have on the quality of life with men who have ED.
Who Can Participate?
Eligibility
Adults ages 18+ who:
- Are diagnosed with ED
- Have an inflatable/malleable implanted device that is used to treat ED
For more information about who can join this study, please contact the study team at urologyresearch@duke.edu.
- Are diagnosed with ED
- Have an inflatable/malleable implanted device that is used to treat ED
For more information about who can join this study, please contact the study team at urologyresearch@duke.edu.
Age Range
18-110
Sex/Genders
Male (cisgender)
Looking for Healthy Participants
No
What is Involved?
If you choose to join this study, you will:
- Fill out questionnaires at various time points after your operation (6 months afterward, 12 months afterward, and then once per year)
- Have information about your penile prosthesis device collected and entered into a database
- Fill out questionnaires at various time points after your operation (6 months afterward, 12 months afterward, and then once per year)
- Have information about your penile prosthesis device collected and entered into a database
Locations
Duke Raleigh Hospital
Visit Timing
Weekdays
Compensation
Yes
Spanish Materials Available
Yes
Study Details
Full Title
It MATTERS - The Erectile Restoration Registry
Principal Investigator
Aaron
Lentz
Protocol Number
PRO00108660
NCT ID
NCT04200937
Phase
N/A
Enrollment Status
OPEN TO ACCRUAL