Evaluating non-surgical treatments for urinary incontinence in women

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to assess the effectiveness of conservative treatments for urinary incontinence in women by examining their impact on symptoms and quality of life. The study will utilize both subjective and objective measures, including self-reported symptoms, bladder diaries, pad tests, and urodynamic studies to evaluate improvements. The focus is on first-line treatments such as behavioral therapy and pelvic floor muscle training, which are recommended to avoid the complications and costs associated with surgical options.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Adult female patient diagnosed with urinary incontinence through clinical assessment
* Diagnosed at Mackay Memorial Hospital and underwent non-surgical treatment and subsequent follow-up.

Exclusion Criteria:

* Choosing invasive or surgical treatment options (such as bladder botulinum toxin injection, urethral sling surgery).
* Unable to comply with regular follow-up for at least one year.
* Pregnant women
* Patients with a history of neuromuscular disorders.

Where it's running

• Department of Obstetrics and Gynecology
  New Taipei City, Taiwan Recruiting

Study contacts

• Study coordinator: Hui-Hsuan Lau, M.D.
• Email: huihsuan1220@gmail.com
• Phone: +886-975-835928

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Other studies for the same condition or treatment. Recruiting studies are listed first.

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• Multimodal approach to reduce urinary incontinence in young female athletes

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.