Actively Recruiting
Stress Urinary Incontinence and Sarcopenia in Postmenopausal Osteoporosis
Led by Beylikduzu State Hospital · Updated on 2024-12-12
100
Participants Needed
1
Research Sites
8 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The primary aim of our study is to evaluate the presence of stress urinary incontinence in postmenopausal patients with and without osteoporosis, determine its impact on quality of life, and explore its relationship with sarcopenia.
CONDITIONS
Official Title
Stress Urinary Incontinence and Sarcopenia in Postmenopausal Osteoporosis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Postmenopausal women with DXA measurements performed within the last 6 months
- Femoral neck and L1-L4 T-scores of -1 and above for the control group (non-osteoporotic)
- Femoral neck and L1-L4 T-scores of -2.5 and below for the osteoporosis group
- Aged 50 to 75 years
You will not qualify if you...
- Refusal to participate in the study
- History of neurological diseases, infections, surgeries, or trauma causing urinary incontinence or muscle loss
- Presence of psychiatric disorders
- Cognitive impairments
- Use of medications that could affect the study results
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Beylikdüzü State Hospital
Istanbul, Turkey (Türkiye), 34147
Actively Recruiting
Research Team
B
Büşra Şirin Ahısha, MD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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