Pharmacologic Effect for Female Overactive Bladder Syndrome: Mirabegron Versus Solifenacin

  • STATUS
    Recruiting
  • End date
    Dec 31, 2022
  • participants needed
    120
  • sponsor
    Far Eastern Memorial Hospital
Updated on 23 March 2022

Summary

To assess the impact of mirabegron versus solifenacin on psychological distress, sexual function, bladder wall thickness and bladder blood flow.

Description

To assess the impact of mirabegron versus solifenacin on psychological distress, sexual function, bladder wall thickness and blood flow.

Details
Condition Overactive Bladder Syndrome
Treatment mirabegron, Solifenacin
Clinical Study IdentifierNCT04023253
SponsorFar Eastern Memorial Hospital
Last Modified on23 March 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

Overactive bladder syndrome

Exclusion Criteria

Allergy to mirabegron or solifenacin
Patients with severe hypertension who are difficult to control, known urethral diverticulum, known bladder malignant tumors, urinary retention patients, gastric retention patients, uncontrolled angular glaucoma patients, dialysis patients, severe renal dysfunction , moderate liver dysfunction, use strong inhibitors of CYP3A4 such as ketoconazole
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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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