Study to Assess the Safety and Efficacy of a Single Treatment of BOTOX in Female Participants with Interstitial Cystitis/Bladder Pain Syndrome (IC/BPS)

Go Back to All Clinical Trials

Study to Assess the Safety and Efficacy of a Single Treatment of BOTOX in Female Participants with Interstitial Cystitis/Bladder Pain Syndrome (IC/BPS)

Are you eligible to participate in this study?

You may be eligible for this study if you meet the following criteria:

Conditions:
Interstitial Cystitis/bladder Pain Syndrome (ic/bps)
Age: Between 18 years - 75 years
Gender: Female

Other Inclusion Criteria:
1. IC/BPS for at least 6 months and confirmed dominant bladder-derived pain, without Hunner lesions.

You may not be eligible for this study if the following are true:

1. Anything other than a positive response to the inclusion criteria above will result in exclusion from study participation.

Contact the research team to learn more about this study.

Your Email

Not a valid e-mail address

Please Provide Email Address

First Name

First name is mandatory

Last Name

Your Phone

Please provide phone number

Invalid phone number

Valid phone number

Comments

Send Confirmation of This To Me

By clicking "Contact Research Team", your contact information will be sent securely to the research staff associated with the study. You will also receive a copy of this email in your inbox, as well as other notifications to determine your participation status in the study.

Clinical Research Studies