Self-Start Triage Model for Post-Botox® Lower Urinary Tract Symptoms

Recruiting Early Phase 1 Interventional Study
Overactive Bladder
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Female
Trial phase
Early Phase 1
Study type
Interventional
Purpose
Supportive Care
Participants needed
260 (estimated)
Sponsor
The Cleveland Clinic · Other
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About This Trial
The primary objective of this study is to investigate whether providing a standing, take-home prescription for empiric Macrobid (self-start model) is superior to standard call-in/urgent care triage (triage model) among patients undergoing intradetrusor Botox®. Urinary tract infections. (UTIs) are the most common complication with intradetrusor Botox®, and patients have to call in to the triage lin…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Female patients of all races and ethnicities aged 18 years and older. * Diagnosis of Overactive Bladder (OAB) and/or Urge Urinary Incontinence (UUI). * Scheduled to receive intradetrusor onabotulinumtoxinA (Botox®) for symptom management. * Has decision making capacity to prov…
Contacts

Ugochukwu Okoroafor, MD

440-799-7739

okoroau@ccf.org

CONTACT

Shannon Wallace, MD

216-444-6878

wallacs8@ccf.org

CONTACT