Examining the link between adenomyosis/myoma and urinary symptoms
The Association Between Adenomyosis/Uterine Myoma and Lower Urinary Tract Symptoms and Gastrointestinal Symptoms
This study is testing how adenomyosis or uterine fibroids might affect bladder, sexual, and bowel function in women compared to those without these conditions.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 150 (estimated) |
| Ages | 20 Years and up |
| Sex | Female |
| Sponsor | Far Eastern Memorial Hospital Academic / other |
| Locations | 1 site (Banqiao, New Taipei) |
| Trial ID | NCT02495311 on ClinicalTrials.gov |
What this trial studies
This observational study aims to investigate the relationship between adenomyosis or uterine myoma and lower urinary tract symptoms, sexual function, and gastrointestinal symptoms in women. Participants with uterine myoma larger than 3 cm or diagnosed with adenomyosis will undergo ultrasonography to assess the size and location of their condition. They will complete various questionnaires related to bladder function, sexual function, and bowel incontinence. A control group of women without these conditions will also be included for comparison.
Who should consider this trial
Good fit: Ideal candidates include women over 20 years old with uterine myoma larger than 3 cm or diagnosed with adenomyosis.
Not a fit: Patients with lower urinary tract infections, acute intestinal inflammation, or a history of bladder or urethra surgery may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance understanding of how adenomyosis and uterine myoma affect urinary and sexual health, leading to better management strategies for affected patients.
How similar studies have performed: While this study explores a specific relationship, similar studies have shown varying degrees of success in understanding the impacts of uterine conditions on urinary symptoms.
Eligibility criteria
Show full inclusion / exclusion criteria
\<Women with myoma or adenomyosis\> Inclusion Criteria: 1. \>20 years old. 2. Myoma: women with \>3 cm uterine myoma 3. Adenomyosis: women with uterus having several dark area (lacunar areas) in one uterine wall or thickening uterine wall \<The control group\> Inclusion criteria: 1. \>20 years old. 2. Women without myoma or adenomyosis \<Both groups\> Exclusion Criteria: 1. The patient has a lower urinary tract infection or acute intestinal inflammation. 2. Previous surgery for the bladder or urethra. 3. History of urinary tract stones or tumors.
Where this trial is running
Banqiao, New Taipei
- Far-Eastern Memorial Hospital — Banqiao, New Taipei, Taiwan (Recruiting)
Study contacts
- Principal investigator: Sheng-Mou Hsiao, MD — Department of Obstetrics & Gynecology, Far Eastern Memorial Hospital, Banqiao, New Taipei, Taiwan
- Study coordinator: Sheng-Mou Hsiao, MD
- Email: smhsiao2@gmail.com
- Phone: +89667000
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.