Study to Gather Information About the Actual Use of an Adhesive Patch Placed on the Skin to Deliver Oxytrol Through the Skin Into the Bloodstream.
Completed · Phase 3
Conditions studied: Overactive Bladder
In brief
With this study researchers want to gather information about the consumer use behavior of Oxytrol in a simulated setting in which the medicine is sold directly to a consumer without a prescription from a healthcare professional. An area of focus was on the potential benefits of an over-the-counter status for Oxytrol and on the ongoing use behavior of the consumers. Oxytrol is a thin, flexible, clear patch that is indicated for the treatment of overactive bladder a disease characterized by a collection of symptoms, including urinary frequency, urgency, and urge incontinence. The adhesive patch is placed on the skin to deliver Oxytrol through the skin into the bloodstream.
Key facts
- Study ID
- NCT04534491
- Run by
- Bayer
- People needed
- 855
- Starts
- 2010-05-25
- Expected to finish
- 2011-06-22
- Last updated by the study team
- 2020-10-20
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Female
- 18 years of age or older
- Not pregnant or suspected to be pregnant
- Never trained or employed as a healthcare professional
- Neither the subject nor anyone in their household worked for a pharmaceutical company, a pharmacy, a managed care or health insurance company, a healthcare practice, or as a healthcare professional
- Had not participated in any market research study, product label study or clinical trial in the past 12 months
You may not qualify if…
- Symptoms of blood in the urine not related to menses
- Back pain and fever in conjunction with frequency or urgency and any of the following: dysuria, hematuria, or cloudy urine
- Narrow-angle glaucoma
- Pregnant (as determined by a urine pregnancy test among women of child bearing potential)
- Breastfeeding
- Known allergy to oxybutynin
Where it is running
- Stevenson Family Pharmacy — Saint Joseph, Missouri, United States
Full record on ClinicalTrials.gov
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