Build status - In Progress
Study to Evaluate Vibegron on Patient Treatment Satisfaction Quality of Life and Healthcare Resource Utilization in Patients with Overactive Bladder
Recruiting
18 years - 99 years
All
20 participants needed
1 Location
Brief description of study
The purpose of this study is to understand:
• If you’re satisfied using GEMTESA ® (Vibegron)
• What side effects (if any) you may experience using GEMTESA ® (Vibegron)
• How GEMTESA ® (Vibegron) impacts your quality of life,
• If you need any additional treatment for Overactive Bladder (OAB) besides GEMTESA® (Vibegron).
.
Participation in the study is expected to last up to 12 months (1 year) but can be extended to 24 months (2 years).
Compensation maximum $200.
Eligibility of study
You may be eligible for this study if you meet the following criteria:
- Conditions: Overactive Bladder
-
Age: 18 years - 99 years
-
Gender: All
Updated on
04 Aug 2024.
Study ID: 851067
Find a site
,
Your Information has been sent successfully.
We have submitted the contact information you provided to the research team at {{SITE_NAME}}. A copy of the message has been sent to your email for your records.
Would you like to be notified about other trials? Sign up for Patient Notification Services.
Sign up
Send a message
Enter your contact details to connect with study team
Primary Contact
Interested in the study
Select a study center that’s convenient for you, and get in touch with the study team.
Contact a study centerPlease choose between Voice or SMS based delivery of verification code
or